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Integrity Delivery Instrument, Tissue Tack 6000120

by Anika Therapeutics, Inc. 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817337000661 UDI-DI Date10 Sep 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Integrity Delivery Instrument, Tissue Tack
Generic Name
Orthopaedic inorganic implant inserter/extractor, single-use
Model / Reference
6000120
Primary DI / UDI-DI
00817337000661
510(k) Number
FDA Product Code
GDW
GMDN Term
Orthopaedic inorganic implant inserter/extractor, single-use
Device Class
Class II
Regulation Number
878.4750
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K222487)

Other devices from Anika Therapeutics, Inc.

See all devices from Anika Therapeutics, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No