Medical Device Manufacturer · US , South Bend , IN

Heraeus Kulzer,GmbH - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2004

Total

Cleared

Denied

Heraeus Kulzer,GmbH has 10 FDA 510(k) cleared dental devices. Based in South Bend, US.

Historical record: 10 cleared submissions from 2004 to 2009.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Heraeus Kulzer,GmbH

10 devices

1-10 of 10

CUTTERSIL ACTIVATOR UNIVERSAL PLUS

RETENTION FLOW OPAQUE

IBOND NEXT GENERATION

HERADOR EC, PF, C, H, NH, G, GG AND MP

K034049 · EJT

Dental · 62d

Heraeus Kulzer,GmbH - FDA 510(k) Cleared Devices

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