Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007006186

FEI Number

3007006186

Entity Name

PROCESS FOR PRF SARL

City/State/Country

Nice Alpes-Maritimes, FR

Establishment Address

49, rue Gioffredo, Nice Alpes-Maritimes 06000, FR

Establishment Type(s)

Foreign Private Label Distributor

Owner / Operator

Process For Prf Sarl (Owner Number: 10045262)

Owner / Operator Contact Address

49, Rue Gioffredo, Nice, FR-06 06000, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

A-PRF Double Spoon PAD A-PRF Tourniquet PomCol INSTRUMENTS PRF Tube holder Bowl Big Compactor SMALL Compactor Bowl PomSwing Tube holder POMPAC Soft Tissue Brush Monoglyc / Glycolon PRF DUO PRF BOX STORAGE BOX

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JZE	Spoon, Ear	Ear, Nose, Throat	Class 1	874.4420	2015-01-15
GAX	Tourniquet, Nonpneumatic	General, Plastic Surgery	Class 1	878.5900	2015-01-15
MDM	Instrument, Manual, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2015-01-15
EMJ	Elevator, Surgical, Dental	Dental	Class 1	872.4565	2018-06-07
GAM	Suture, Absorbable, Synthetic, Polyglycolic Acid	General, Plastic Surgery	Class 2	878.4493	2022-06-22
QBV	Centrifuge For Preparation Of Cell Concentrate And/Or Plasma Concentrate	Clinical Chemistry	Class 1	862.2050	2023-09-18
LXG	Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use	Clinical Chemistry	Class 1	862.2050	2014-02-06

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Process For Prf Sarl

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K123940	Demetech Corp.	DEMEQUICKTM (RAPID ABSORBABLE) SYNTHETIC SURGICAL SUTURE	2014-05-30
K050845	ETHICON, Inc.	MONOCRYL PLUS ANTIBACTERIAL SUTURE	2005-06-29

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0010-2021	Riverpoint Medical, LLC	2	Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 6/0 Undyed 18" P-10 Cutting, Product Number: SV9913, UDI: 20884521153278 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures.
Z-0011-2021	Riverpoint Medical, LLC	2	Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" P-14 Cutting, Product Number: SV935, UDI: 20884521151755 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures.
Z-0012-2021	Riverpoint Medical, LLC	2	Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" P-12 Cutting, Product Number: SV426, UDI: 20884521151731 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures.
Z-0013-2021	Riverpoint Medical, LLC	2	Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36" KV-34 TaperCutting, Product Number: CV919, UDI: 20884521151649 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures.
Z-0014-2021	Riverpoint Medical, LLC	2	Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" C-12 Cutting, Product Number: SV2294, UDI 20884521151403 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation, ophthalmic, cardiovascular or neurological procedures.

Similar Registrations

Registration Number	Establishment Name	Location
9613083	TOWNE BROTHERS (PVT.), LTD.	SIALKOT Punjab, PK
3008808049	SURGICRAFTS	Sialkot Punjab, PK
9611102	RICHARD WOLF GMBH	KNITTLINGEN Baden-Wurttemberg, DE
3004001706	BR SURGICAL LLC	Jacksonville, FL, US
3003902419	DALIAN WENJING WOODEN INDUSTRY CO., LTD.	DALIAN Liaoning, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007006186. Last updated year: 2026. Please use registration number 3007006186 when referencing this establishment in official correspondence.