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Tissue Punch 5mm Tissue Punch

by Oco Biomedical

Tissue Punch 5mm Tissue Punch (0065) is a Class I device made by Oco Biomedical, listed in FDA GUDID since 21 Apr 2016 (UDI-DI D7850065TP0), 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 NumberD7850065TP0 UDI-DI Date21 Apr 2016ListedStatusListed 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  • Withdrawn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
Tissue Punch
Generic name
Dental soft-tissue coring punch, reusable
Model / Ref / Catalog
5mm Tissue Punch, 0065
Primary DI / UDI-DI
D7850065TP0
FDA product code
DZN
GMDN term
Dental soft-tissue coring punch, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Properties

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