Medical Device Manufacturer · CA , Winnipeg, Manitoba

Verg, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1996

Total

Cleared

Denied

Verg, Inc. has 1 FDA 510(k) cleared medical devices. Based in Winnipeg, Manitoba, CA.

Historical record: 1 cleared submissions from 1996 to 1996. Primary specialty: General & Plastic Surgery.

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

Verg, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Verg, Inc.

1 devices

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