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ProCure PCBB2000

by Twin Med, LLC

ProCure PCBB2000 is a Class I device made by Twin Med, LLC, listed in FDA GUDID since 14 Nov 2024 (UDI-DI 10840330701362), 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 Number10840330701362 UDI-DI Date14 Nov 2024ListedStatusListed 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  • Withdrawn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
ProCure
Generic name
Pill crusher/splitter
Model / Ref / Catalog
PCBB2000
Primary DI / UDI-DI
10840330701362
FDA product code
FNY
GMDN term
Pill crusher/splitter
Device class
Class I
Regulation number
880.6730
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pill crusher/splitter

Similar devices

Other devices filed under FDA product code FNY (Basin, Emesis).

Other devices from Twin Med, LLC

See all devices from Twin Med, LLC →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (10, all answered No)