Medical Device Manufacturer · US , Bend , OR

Zhermack S.P.A. - FDA 510(k) Cleared Devices

19 submissions · 19 cleared · Since 1996

Total

Cleared

Denied

Zhermack S.P.A. has 19 FDA 510(k) cleared dental devices. Based in Bend, US.

Historical record: 19 cleared submissions from 1996 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.

Zhermack S.P.A. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Zhermack S.P.A.

19 devices

1-19 of 19

Cleared Mar 26, 2009

HYDRORISE AND HYDROSYSTEM

NEOCOLLOID, ORTHOPRINT

ELITE H-D VINYL POLYSILOXANE IMPRESSION MATERIALS .PUTTY SOFT/NORMAL SETTING...

K972239 · ELW

Dental · 46d

Cleared Jul 16, 1997

ELITE H-D HYDROPHILIC VINYL POLYSILOXANE IMPRESSION MATERIALS (LIGHT...

Zhermack S.P.A. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Zhermack S.P.A.

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