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CarriGen ® 76-6036

by Etex Corp.

CarriGen ® 76-6036 is a Class I device made by Etex Corp., listed in FDA GUDID since 24 Oct 2015 (UDI-DI 00889024205567), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00889024205567 UDI-DI Date24 Oct 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
CarriGen ®
Generic name
Synthetic bone graft
Model / reference
76-6036
Primary DI / UDI-DI
00889024205567
FDA product code
LYV, MQV, MBP, LYC
GMDN term
Synthetic bone graft
Device class
Class I
Regulation number
878.4800, 888.3045, 872.3930
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 10 Milliliter

Related devices

Category: Synthetic bone graft

Similar devices in this category

Other devices filed under Synthetic bone graft.

Other devices from Etex Corp.

See all devices from Etex Corp. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)