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Consepsis 2210

by Ultradent Products, Inc.

Consepsis 2210 is a Class II device made by Ultradent Products, Inc., listed in FDA GUDID since 22 Sep 2016 (UDI-DI 00883205106322), 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 Number00883205106322 UDI-DI Date22 Sep 2016ListedStatusListed 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  • Withdrawn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
Consepsis
Generic name
Dental tooth-cleaning solution
Model / Ref / Catalog
2210
Primary DI / UDI-DI
00883205106322
FDA product code
LBH
GMDN term
Dental tooth-cleaning solution
Device class
Class II
Regulation number
872.3260
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LBH (VARNISH, CAVITY).

Other devices from Ultradent Products, Inc.

See all devices from Ultradent Products, Inc. →

Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)