FDA device listing

200147 Finishing & polishing kit ceramics/composites,50500 REDUCERS HP, pu: 2pcs,50510 REDUCERS CA, pu: 2 pcs,50520…

FDA device listing 1354004574 · DFS-DIAMON GMBH

Key facts

Proprietary names 200147 Finishing & polishing kit ceramics/composites,50500 REDUCERS HP, pu: 2pcs,50510 REDUCERS CA, pu: 2 pcs,50520 REDUCERS HP-FG 1,6 mm, pu: 2 pcs,800209 ZIRCONIA TOOL KIT,80023 Circopol A,80024 Circopol B,800559 Polisher Durocomp large torpedo CA, pu: 6 pcs,800569 Polisher Durocomp small torpedo CA, pu: 6 pcs,800579 Polisher Durocomp lense CA, pu: 6 pcs,800589 Polisher Durocomp cup CA, pu: 6…
Owner/operator DFS-DIAMON GMBH
Owner/operator number 9031482
Product codes DZP
Device names DZP - Instrument, Diamond, Dental
Device class Class I
Classification regulations (21 CFR) 872.4535
Review panels Dental
Registered establishments DFS-DIAMON GMBH
Establishment registrations 9614948
FEI numbers 3000283415
Establishment operations Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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