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Toejack TJB-1001T-DPG

by Nvision Biomedical Technologies, Inc

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810135961233 UDI-DI Date29 Jul 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  • Withdrawn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
Toejack
Generic name
Dental implantation depth/angle gauge, reusable
Model / reference
TJB-1001T-DPG
Description
ToeJack Depth Gauge Body ToeJack Depth Gauge Measurement Rod ToeJack Depth Gauge Stopper ToeJack K-wire Depth Gauge
Primary DI / UDI-DI
00810135961233
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

Other devices from Nvision Biomedical Technologies, Inc

See all devices from Nvision Biomedical Technologies, Inc →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number

Other properties (11)

  • Supplied sterile: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No