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Staydent NS 5501C

by Sheffield Pharmaceuticals LLC

Staydent NS 5501C (17024024) is a Class I device made by Sheffield Pharmaceuticals LLC, listed in FDA GUDID since 9 Jun 2025 (UDI-DI 00732953170249), 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 Number00732953170249 UDI-DI Date9 Jun 2025ListedStatusListed 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  • Withdrawn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
Staydent
Generic name
Carboxymethylcellulose sodium/polymer denture adhesive, zinc-free
Model / Ref / Catalog
NS 5501C, 17024024
Primary DI / UDI-DI
00732953170249
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 Sheffield Pharmaceuticals LLC

  • LubriGel 5442103

    Class II

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)