Medical Device Manufacturer · CA , Guelph, Ontario

The Helene Edgar Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1995

Total

Cleared

Denied

The Helene Edgar Corp. has 1 FDA 510(k) cleared medical devices. Based in Guelph, Ontario, CA.

Historical record: 1 cleared submissions from 1995 to 1995. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by The Helene Edgar Corp. Filter by specialty or product code using the sidebar.

The Helene Edgar Corp. 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 - The Helene Edgar Corp.

1 devices

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