Medical Device Manufacturer · CA , Boucherville, Quebec

Skeltex Technologies, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2010

Total

Cleared

Denied

Skeltex Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Boucherville, Quebec, CA.

Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Orthopedic.

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

Skeltex Technologies, 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 - Skeltex Technologies, Inc.

1 devices

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