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Dental City 34-932140

by Icp, Inc.

Dental City 34-932140 is a Class I device made by Icp, Inc., listed in FDA GUDID since 27 May 2026 (UDI-DI D771349321401), 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 NumberD771349321401 UDI-DI Date27 May 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  • Withdrawn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
Dental City
Generic name
Orthodontic inter-arch elastic band
Model / reference
34-932140
Primary DI / UDI-DI
D771349321401
FDA product code
ECI
GMDN term
Orthodontic inter-arch elastic band
Device class
Class I
Regulation number
872.5410
GUDID distribution status
In Commercial Distribution

Other devices from Icp, Inc.

See all devices from Icp, Inc. →

Properties

  • Single use
  • Contains latex
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)