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Gel-E, Inc.

United StatesFDA applicant, unverified

Devices
3

What Gel-E, Inc. makes

Gel-E, Inc. manufactures over-the-counter (OTC) gel-based products designed for temporary pain relief and muscle recovery, including the gel-e Flex+, gel-e Flex, and gel-e Flex+ variants. These products are formulated for topical application to address localized discomfort and stiffness.

The company’s portfolio is classified under FDA Class II devices and is authorised through 510(k) clearance in the United States. The products are listed in the FDA’s 510(k) registry, adhering to regulatory requirements for medical devices.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • gel-e Flex+ gel OTC Ref K192667

    Active Regimes: 510(k) Registry: 510(k) Class:—

  • gel-e Flex Ref K180152

    Active Regimes: 510(k) Registry: 510(k) Class:—

  • gel-e Flex+ Ref K182811

    Active Regimes: 510(k) Registry: 510(k) Class:—

Frequently asked questions

How many devices does Gel-E, Inc. have in the registry?

The registry currently lists 3 devices for Gel-E, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Gel-E, Inc.'s devices?

Among its 3 most recently registered devices, Gel-E, Inc. has devices listed in FDA 510(k) (3 devices).

What are the newest devices from Gel-E, Inc. in the registry?

The most recently registered devices listed for Gel-E, Inc. include gel-e Flex+ gel OTC, gel-e Flex and gel-e Flex+.

Generated automatically from registry data and not verified by a human reviewer.