Medical Device Manufacturer · US , Raleigh , NC

Merz North America, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

Total

Cleared

Denied

Merz North America, Inc. has 1 FDA 510(k) cleared medical devices. Based in Raleigh, US.

Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Merz North America, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Merz North America, Inc.

1 devices

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