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OSSIO® Tap THN00642

by Ossio Ltd

OSSIO® Tap THN00642 is a Class I device made by Ossio Ltd, listed in FDA GUDID since 19 Jul 2026 (UDI-DI 07290019361381), 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 Number07290019361381 UDI-DI Date19 Jul 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  • Withdrawn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
OSSIO® Tap
Generic name
Bone tap, single-use
Model / Ref / Catalog
THN00642
Primary DI / UDI-DI
07290019361381
FDA product code
HWX
GMDN term
Bone tap, single-use
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HWX (Tap, Bone).

Other devices from Ossio Ltd

See all devices from Ossio Ltd →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)