Gel-E, Inc. (Formerly Remedium Technologies, Inc.)
Country not established
- Devices
- 1
What Gel-E, Inc. (Formerly Remedium Technologies, Inc.) makes
Gel-E, Inc. manufactures the gel-e Bandage, a wound care product designed for managing and treating minor to moderate wounds, including burns, abrasions, and surgical incisions. The bandage incorporates a hydrogel-based gel to maintain a moist wound environment, promoting healing while providing protection against infection and dehydration.
The gel-e Bandage is classified as a Class II device under FDA regulations and has undergone 510(k) clearance. The product is listed in the FDA’s 510(k) database, adhering to U.S. medical device compliance standards. The company is headquartered in the United States.
Catalogue
gel-e Bandage Ref K172010
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gel-E, Inc. (Formerly Remedium Technologies, Inc.) have in the registry?
The registry currently lists 1 device for Gel-E, Inc. (Formerly Remedium Technologies, Inc.). Devices recorded under merged duplicate company entries are counted once.
Which registries list Gel-E, Inc. (Formerly Remedium Technologies, Inc.)'s devices?
Among its 1 most recently registered device, Gel-E, Inc. (Formerly Remedium Technologies, Inc.) has devices listed in FDA 510(k) (1 device).
What are the newest devices from Gel-E, Inc. (Formerly Remedium Technologies, Inc.) in the registry?
The most recently registered devices listed for Gel-E, Inc. (Formerly Remedium Technologies, Inc.) include gel-e Bandage.