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TendMIN® Anchor Kit TK-01-A

by Astron Medtech Co., Ltd

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04719899650000 UDI-DIDate9 Sep 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
TendMIN® Anchor Kit
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable
Model / Ref / Catalog
TK-01-A
Primary DI / UDI-DI
04719899650000
GMDN Term
Tendon/ligament bone anchor, non-bioabsorbable
GUDID distribution status
In Commercial Distribution

Other devices from Astron Medtech Co., Ltd

Properties

  • Single Use
  • Implantable
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Sterile: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No