System comparison

Emcyte PurePRP vs Selphyl

These are not two versions of the same product. Emcyte PurePRP SP prepares liquid platelet-rich plasma. Selphyl prepares PRFM, a platelet-rich fibrin matrix, by adding calcium chloride to convert the plasma into a fibrin scaffold. Before you compare specifications, decide which of those two things your protocol actually calls for.

Disclosure: PRP Direct is an Emcyte distributor. We have a commercial interest in one of the systems on this page. Every Selphyl figure below is quoted from Selphyl's own published material with a link and a date, including their growth-factor claim, which we attribute to them rather than restate or dispute. We do not make efficacy claims for our own products either.

The category difference comes first

Selphyl describes its output as Platelet-Rich Fibrin Matrix and positions it as the next generation of PRP. Mechanically, the system draws blood into a proprietary tube with a separator gel, spins once for about six minutes, transfers the plasma through a closed system into a second tube containing calcium chloride, and the calcium triggers fibrin polymerization that converts the PRP into a matrix.

That last step is the whole distinction. A liquid you inject and a polymerized matrix behave differently in the syringe, in the tissue, and in how you plan a case. Our PRP vs PRF guide covers what changes when fibrin forms.

So the honest first question is not "which is more concentrated." It is whether you want a measurable liquid dose or a fibrin scaffold. If it is the scaffold, we are not your supplier, and we would rather tell you that here than after you have spent an hour on a call.

Side by side

Selphyl figures are as published by Selphyl. Emcyte figures are manufacturer-reported. Rows are matched only where the two publish comparable information.

SpecificationEmcyte PurePRP SPSelphyl
What it producesLiquid platelet-rich plasmaPlatelet-Rich Fibrin Matrix (PRFM)
Spins21, approximately 6 minutes
Conversion stepNone; output stays liquidPlasma transferred into a calcium chloride tube; fibrin polymerization
Cell separation methodDensity separation across two spinsSeparator gel; red and white cells retained below the gel
Platelet concentration published≥ 6x baselineNot published as a concentration multiple
Leukocyte profileSelectable, neutrophil-rich or neutrophil-poorWhite cells described as retained below the separator gel
Output volume7 mL from the 60 mL kitNot published; small blood draw described
Kit sizes30 / 60 / 120 mLTube-based kit; sizes not published on the product page
Other preparations on the same platformBone marrow concentrate, adipose, A2M ultrafiltrationNot published
Growth-factor releaseNo release-duration claim madeSelphyl states growth factors are released up to 7 days versus hours with traditional PRP

Selphyl specifications and claims from selphyl.com (retrieved 2026-07-25), including the kit component list and the process description. The growth-factor release figure is Selphyl's own published claim, reproduced here as their statement. We have not independently evaluated it, and we make no competing release-duration claim for any product we sell. Emcyte specifications are manufacturer-reported. Rows marked not published are left that way because the manufacturer does not publish that figure on its public product page.

On the seven-day claim

Selphyl's central marketing argument is sustained growth-factor release from the fibrin matrix. We are not going to tell you it is wrong, because we have not evaluated it and it is not our claim to adjudicate. The mechanism it describes, a fibrin scaffold binding platelets and releasing over time, is a real and widely discussed rationale in the literature.

What we will say is what applies to every claim in this category, including ours: a mechanism is not an outcome, release kinetics measured in a tube are not a clinical result, and no PRP or PRFM preparation is FDA-approved to treat any condition. Ask any supplier, us included, to show you where a number came from and who paid for the study.

Where each one fits

  • Selphyl fits aesthetic practices that specifically want a fibrin matrix rather than a liquid, and want a short single-spin workflow with a small draw.
  • PurePRP SP fits practices injecting a measurable liquid dose, wanting a selectable leukocyte profile, or running orthopedic, bone marrow, and adipose cases on one centrifuge.
  • If you are unsure which category you need, read the PRP vs PRF guide first. That decision determines the supplier, not the other way around.

Common questions

Is Selphyl the same as PRP?

Not quite. Selphyl produces PRFM, a platelet-rich fibrin matrix, by transferring plasma into a calcium chloride tube so fibrin polymerizes. Emcyte PurePRP produces liquid PRP with no conversion step. Selphyl positions PRFM as the next generation of PRP, but the physical output differs.

Does PRFM really release growth factors for seven days?

That is Selphyl's published claim and we reproduce it as theirs. We have not independently evaluated it and make no competing release-duration claim. Note generally that release kinetics measured in a tube are a mechanism, not a clinical outcome, whoever is making the claim.

Which has higher platelet concentration?

Emcyte publishes at least 6x baseline for PurePRP SP. Selphyl does not publish a concentration multiple on its public product page, so there is no like-for-like comparison to make. We are not going to estimate a number on another manufacturer's behalf.

Does PRP Direct sell Selphyl?

No. We distribute the Emcyte point-of-care line: PRP, bone marrow concentrate, adipose, and the A2M ultrafiltration component. If your protocol specifically calls for a fibrin matrix, we are not the right supplier and will say so.

Need a liquid PRP dose you can measure?

Tell us the cases you run. We'll send itemized pricing on the kits that match, within one business day. No login wall.

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PRP Direct is an Emcyte distributor. Competitor specifications and claims are quoted from the manufacturers' own published materials and are their statements, not ours. Devices referenced are cleared blood-processing devices; clearance covers how a device processes blood and is not a clearance of the prepared PRP or PRFM to treat any condition, and no PRP therapy is FDA-approved for a specific indication. Manufacturer specifications are not claims of clinical efficacy. This page is general education and is not medical advice. Product names and trademarks belong to their respective owners.

What these devices are cleared for

Emcyte's instructions for use define the labeled indication for the PurePRP Supraphysiologic Concentrating System as follows, quoted verbatim:

"The PurePRP® Supraphysiologic Concentrating System is designed to be used for the safe and rapid preparation of autologous platelet rich plasma (PRP) from a small sample of blood at the patient's point of care. The PRP is mixed with autograft and allograft bone prior to application to an orthopedic site to improve bone graft handling characteristics."

The same document states: "The PRP prepared by this device has not been evaluated for any clinical indications." It also states that the safety and effectiveness of the device for in vivo indications such as bone healing and hemostasis have not been established, and that the PRP prepared by the device is not indicated for delivery to the patient's circulatory system.

Any application other than the labeled indication falls outside it. That is not unusual in this field, and it is not something PRP Direct can authorize, recommend, or direct. It rests on the independent clinical judgment of a licensed physician, exercised under their own license and their own informed-consent process. We sell equipment and publish what the manufacturer publishes about it. We do not advise on clinical application.

PRP Direct is a distributor of Emcyte point-of-care blood-processing devices. Emcyte states these systems are 510(k)-cleared as blood-processing devices; clearance covers how a device processes blood, it is not a clearance of the prepared PRP to treat any condition, and no PRP therapy is FDA-approved for a specific indication. Manufacturer specifications are reproduced as the manufacturer's statements, have not been independently verified by PRP Direct, and are not claims of clinical efficacy. Manufacturers revise specifications without notice, and the instructions for use packaged with your kit supersede anything published here. Nothing on this page is dosing, protocol, clinical, or medical advice, and nothing here should be relied upon in making a clinical decision. Product names and trademarks belong to their respective owners.