Skip to content

NuOss XC Socket 5092001

by Collagen Matrix, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00813954027975 UDI-DIDate7 Jan 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
NuOss XC Socket
Generic Name
Dental bone void filling material, animal-derived
Model / Ref / Catalog
5092001
Primary DI / UDI-DI
00813954027975
FDA Product Code
NPM
GMDN Term
Dental bone void filling material, animal-derived
Device Class
Class II
Regulation Number
872.3930
GUDID distribution status
In Commercial Distribution

Other devices from Collagen Matrix, Inc.

See all devices from Collagen Matrix, Inc. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Contains Latex
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (7)

  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No