REVOGEN BIOLOGICS

FDA Device Registration & Listing · San Antonio, TX, US · Registration 3043620406

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3043620406
FEI Number
3043620406
Entity Name
REVOGEN BIOLOGICS
City/State/Country
San Antonio, TX, US
Establishment Address
4903 Golden Quail Ste 120, San Antonio, TX 78240, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Revogen Biologics (Owner Number: 10095019)
Owner / Operator Contact Address
4903 Golden Quail Suite 120, San Antonio, TX 78240, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K173525
PMA Number
N/A

All Registered Proprietary Names

RevoGro

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2026-01-15

Official Correspondent

Randy Peloquin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Revogen Biologics
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
K180121 Cellumed Co., Ltd. Rafugen DBM 2018-04-11
K062691 Takiron Co., Ltd. COMPORUS 2008-04-15
K023703 Berkeley Advanced Biomaterials, Inc. BI-OSTETIC 2003-01-30
K173933 Xenco Medical, LLC Sorrento Bioglass Bone Graft Substitute 2018-09-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043620406. Last updated year: 2026. Please use registration number 3043620406 when referencing this establishment in official correspondence.
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