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CareALL DA85

by New World Imports, Inc.

CareALL DA85 is a Class I device made by New World Imports, Inc., listed in FDA GUDID since 11 Aug 2020 (UDI-DI 00085317005795), 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 Number00085317005795 UDI-DI Date11 Aug 2020ListedStatusListed 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  • Withdrawn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
CareALL
Generic name
Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free
Model / reference
DA85
Primary DI / UDI-DI
00085317005795
FDA product code
KOO
GMDN term
Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free
Device class
Class I
Regulation number
872.3490
GUDID distribution status
In Commercial Distribution

Related devices

Category: Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free

Similar devices

Other devices filed under FDA product code KOO (Adhesive, Denture, Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt).

Other devices from New World Imports, Inc.

See all devices from New World Imports, Inc. →

Properties

  • Premarket exempt
Other properties (14, all answered No)