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Depth Gauge HDG2216

by Ossvis Co., Ltd.

Depth Gauge HDG2216 is a Class I device made by Ossvis Co., Ltd., listed in FDA GUDID since 25 Oct 2023 (UDI-DI 08809877419760), 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 Number08809877419760 UDI-DI Date25 Oct 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  • Withdrawn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
Depth Gauge
Generic name
Dental implantation depth/angle gauge, reusable
Model / reference
HDG2216
Primary DI / UDI-DI
08809877419760
FDA product code
EIL
GMDN term
Dental implantation depth/angle gauge, 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)