Tropocells® PRP System

The Tropocells PRP system helps physicians prepare platelet-rich plasma (PRP) with a simple and consistent process.

First, clinicians collect a patient’s blood. Next, they spin the sample in a centrifuge. Then, the system separates the blood and concentrates platelets in the plasma.

Because PRP comes from the patient’s own blood, it is an autologous biologic. In addition, the system uses sterile, single-use parts and clear spin settings. As a result, clinicians can prepare PRP in their office with a steady and repeatable method.

Transcend Biologics Tropocells PRP

Designed for Consistent Results

The system uses engineered parts to support reliable platelet separation. Because of this, clinicians can expect consistent results across cases.

In addition, the design helps reduce variation between procedures. As a result, teams can follow a more predictable process.

Key features include:

  • sterile, single-use kits
  • gel separator for platelet concentration
  • proprietary anticoagulant for patient comfort
  • anti-stick coating to improve platelet capture
  • point-of-care workflow

Together, these features support a simple and efficient process.

Tropocells PRP Kit
Platelet-rich Plasma

Tropocells PRP System Highlights

The system supports steady platelet concentration and repeatable workflows. In addition, it helps simplify PRP preparation in clinical settings.

Because of this, clinicians can focus more on patient care and less on process variation.

Key characteristics include:

  • nearly 0% red blood cells
  • leukocyte-poor PRP profile
  • physiologic pH
  • simple vacuum blood draw
  • consistent performance
  • efficient platelet concentration
  • up to 4.7× concentration in one spin

Designed for Clinical Use

Clinicians across many specialties use PRP systems. For example, the Tropocells system fits into:

  • orthopedic practices
  • sports medicine clinics
  • pain management centers
  • regenerative medicine practices
  • outpatient facilities

Because these teams already perform injections and blood draws, they can add PRP without major workflow changes. As a result, adoption is straightforward.

platelet rich plasma kit centrifuge preparation

Simple PRP Preparation Workflow

Tropocells blood collection

Collect Patients Blood
(11 mL, 22 mL, or 40 mL) 

Transcend Axis centrifuge

Centrifuge (10 min.) 

Tropocells PRP Separation

Extract Platelet-Poor Plasma (PPP)

PRP collection

Collect Platelet-Rich Plasma (PRP) and apply

Why Clinicians Choose Tropocells® PRP

The Tropocells PRP system supports a simple and predictable process. In addition, it helps improve efficiency in clinical settings.

Because of this, many clinicians choose it for routine PRP preparation.

High Platelet Concentration

80% (+/- 10%) Platelet Yield + customizable concentrations up to 4.5x

Safe & Autologous

FDA Cleared 510(k) Class II Medical Device (BK110035) Non-Pyrogenic – Sterile – Closed System

Monocyte-Dominant profile

System produces PRP in which monocytes outnumber neutrophils

Simple and Predictable Workflow

Small blood draw, single centrifuge spin, reproducible preparation method

Reduced Red Blood Cell Content

Eliminates nearly 100% of red blood cells and 95% of white blood cells

Designed for Patient Comfort

The proprietary MNC7 anticoagulant helps maintain physiologic pH. As a result, clinicians may reduce irritation during injection

System Specifications

The system offers multiple kit sizes. Therefore, clinicians can choose what fits their needs.

  • 11 mL – low volume
  • 22 mL – mid range
  • 40 mL – higher volume

Each option supports consistent separation using the same process. As a result, workflow stays consistent across cases.

prp specifications
prp 7 reasons
prp safety

Safety and Manufacturing Standards

Tropocells® PRP systems follow strict quality standards. In addition, manufacturing occurs in controlled environments.

Production includes:

  • ISO 7 cleanroom environments
  • ISO 5 critical processing areas
  • ISO 13485-certified facilities
  • FDA-registered manufacturing

Independent testing includes:

  • hypersensitivity testing
  • cytotoxicity testing
  • systemic toxicity testing

More than 850,000 clinical uses have been reported since 2013.

Regulatory Status

PRP systems are Class II medical devices under FDA guidelines. Therefore, they must receive 510(k) clearance.

Tropocells® PRP is cleared under BK110035. In addition, the system prepares PRP at the point of care using a small blood sample.

Request Information

Healthcare professionals can contact Transcend Biologics for:

  • product information
  • technical specifications
  • availability

In addition, our team can explain how PRP fits into your workflow. Therefore, you can evaluate whether it meets your practice needs.