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TMA Snap-On TMI0031

by Adin Dental Implant Systems Ltd

TMA Snap-On TMI0031 is a Class I device made by Adin Dental Implant Systems Ltd, listed in FDA GUDID since 26 Oct 2026 (UDI-DI 07290116777931), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290116777931 UDI-DI Date26 Oct 2026ListedStatusListed 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  • Withdrawn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
TMA Snap-On
Generic name
Dental implant suprastructure, temporary, preformed, single-use
Model / reference
TMI0031
Primary DI / UDI-DI
07290116777931
FDA product code
NDP
GMDN term
Dental implant suprastructure, temporary, preformed, single-use
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code NDP (Accessories, Implant, Dental, Endosseous).

Other devices from Adin Dental Implant Systems Ltd

See all devices from Adin Dental Implant Systems Ltd →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (8, all answered No)