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Twist Drill HTD33C

by Ossvis Co., Ltd.

Twist Drill HTD33C is a Class I device made by Ossvis Co., Ltd., listed in FDA GUDID since 13 Dec 2023 (UDI-DI 08809918206625), 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 Number08809918206625 UDI-DI Date13 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  • Withdrawn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
Twist Drill
Generic name
Fixture/appliance dental drill bit, reusable
Model / reference
HTD33C
Primary DI / UDI-DI
08809918206625
FDA product code
DZA
GMDN term
Fixture/appliance dental drill bit, reusable
Device class
Class I
Regulation number
872.4130
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)