Skip to content

FiberFIX 160145-1

by Nanova Biomaterials Inc

FiberFIX 160145-1 is a Class II device made by Nanova Biomaterials Inc, listed in FDA GUDID since 9 Jun 2026 (UDI-DI 00816537023036), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816537023036 UDI-DI Date9 Jun 2026ListedStatusListed 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  • Withdrawn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
FiberFIX
Generic name
Tendon/ligament bone anchor, bioabsorbable
Model / Ref / Catalog
160145-1
Primary DI / UDI-DI
00816537023036
FDA product code
MAI
GMDN term
Tendon/ligament bone anchor, bioabsorbable
Device class
Class II
Regulation number
888.3030
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Other devices from Nanova Biomaterials Inc

See all devices from Nanova Biomaterials Inc →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)