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ProCopper P-120248

by Silmet Ltd

ProCopper P-120248 is a Class II device made by Silmet Ltd, listed in FDA GUDID since 22 Oct 2017 (UDI-DI 07290016787603), 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 Number07290016787603 UDI-DI Date22 Oct 2017ListedStatusListed 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  • Withdrawn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
ProCopper
Generic name
Dental amalgam
Model / Ref / Catalog
P-120248
Primary DI / UDI-DI
07290016787603
FDA product code
EJJ
GMDN term
Dental amalgam
Device class
Class II
Regulation number
872.3070
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental amalgam

Other devices from Silmet Ltd

See all devices from Silmet Ltd →

Properties

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