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M-PM Disc

by Merz Dental GmbH 175 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD7091019102 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Dental appliance fabrication material, thermoplastic
Model / Ref / Catalog
M-PM Disc, PMMA-Disc, shade BL3 translucent thickness 16mm, diameter 98, 5mm, 1019102
Primary DI / UDI-DI
D7091019102
510(k) Number
FDA Product Code
EBG
GMDN Term
Dental appliance fabrication material, thermoplastic
Device Class
Class II
Regulation Number
872.3770
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 98.5 Millimeter
Height — 16 Millimeter

Related devices

Category: Temporary dental crown/bridge

Cleared under the same submission (K071548)

Show all (12)

Other devices from Merz Dental GmbH

See all devices from Merz Dental GmbH →

Properties

  • Lot / Batch Number
  • Expiration Date

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No