FiberFIX 90923-1

by Nanova Biomaterials Inc

FiberFIX 90923-1 is a Class II device made by Nanova Biomaterials Inc, listed in FDA GUDID since 21 Aug 2021 (UDI-DI 00816537021759), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00816537021759 UDI-DI	Date21 Aug 2021Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00816537021759

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: FiberFIX
Generic name: Bioabsorbable orthopaedic bone screw
Model / reference: 90923-1

Primary DI / UDI-DI: 00816537021759
FDA product code: MAI
GMDN term: Bioabsorbable orthopaedic bone screw

Device class: Class II
Regulation number: 888.3030
GUDID distribution status: In Commercial Distribution

Sterilisation method: Ethylene Oxide

Similar devices in this category

Other devices filed under Bioabsorbable orthopaedic bone screw.

Other devices from Nanova Biomaterials Inc

FiberFIX 160129-1

Class II
FiberFIX 160135-1

Class II
FiberFIX 160145-1

Class II
FiberFIX 190145-1

Class II

See all devices from Nanova Biomaterials Inc →

Properties

Supplied sterile
Sterilise before use
Single use
Implantable
Prescription use
Lot / batch number
Expiration date

Other properties (8, all answered No)