Medical Device Manufacturer · US , College Park , MD

Gel-E, Inc. (Formerly Remedium Technologies, Inc.) - FDA 510(k) Clear...

1 submissions · 1 cleared · Since 2017

Total

Cleared

Denied

Gel-E, Inc. (Formerly Remedium Technologies, Inc.) has 1 FDA 510(k) cleared medical devices. Based in College Park, US.

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

Browse the FDA 510(k) cleared devices submitted by Gel-E, Inc. (Formerly Remedium Technologies, Inc.) Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Gel-E, Inc. (Formerly Remedium Technologies, Inc.)

1 devices

1-1 of 1

Cleared Dec 07, 2017

gel-e Bandage

K172010 · KGN

General & Plastic Surgery · 157d

Gel-E, Inc. (Formerly Remedium Technologies, Inc.) - FDA 510(k) Clear...

FDA 510(k) Regulatory Record - Gel-E, Inc. (Formerly Remedium Technologies, Inc.)

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