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Bone Tack Carrier HSBC

by Ossvis Co., Ltd.

Bone Tack Carrier HSBC is a Class I device made by Ossvis Co., Ltd., listed in FDA GUDID since 15 Dec 2023 (UDI-DI 08809918209619), 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 Number08809918209619 UDI-DI Date15 Dec 2023ListedStatusListed 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  • Withdrawn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
Bone Tack Carrier
Generic name
Bone tack inserter, basic
Model / reference
HSBC
Primary DI / UDI-DI
08809918209619
FDA product code
NDP
GMDN term
Bone tack inserter, basic
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code NDP (Accessories, Implant, Dental, Endosseous).

Other devices from Ossvis Co., Ltd.

See all devices from Ossvis Co., Ltd. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)