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Plasdent UCMN-2P

by Plasdent Corp.

Plasdent UCMN-2P is a Class I device made by Plasdent Corp., listed in FDA GUDID since 28 Jan 2022 (UDI-DI D832UCMN2P0), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD832UCMN2P0 UDI-DI Date28 Jan 2022ListedStatusListed 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  • Withdrawn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
Plasdent
Generic name
Dental impression material syringe, reusable
Model / Ref / Catalog
UCMN-2P
Primary DI / UDI-DI
D832UCMN2P0
FDA product code
EID
GMDN term
Dental impression material syringe, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental impression material syringe, reusable

Other devices from Plasdent Corp.

See all devices from Plasdent Corp. →

Properties

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