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Dentemp 1

by Doc Brands, Inc.

Dentemp 1 is a Class I device made by Doc Brands, Inc., listed in FDA GUDID since 9 Mar 2022 (UDI-DI 00372494101854), 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 Number00372494101854 UDI-DI Date9 Mar 2022ListedStatusListed 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  • Withdrawn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
Dentemp
Generic name
Home-use dental cement
Model / reference
1
Primary DI / UDI-DI
00372494101854
FDA product code
EMB
GMDN term
Home-use dental cement
Device class
Class I
Regulation number
872.3275
GUDID distribution status
In Commercial Distribution
Size
Weight — 2.64 Gram

Related devices

Category: Home-use dental cement

Other devices from Doc Brands, Inc.

See all devices from Doc Brands, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)