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Tactyl Technologies, Inc.

United StatesFDA applicant, unverified

Devices
7

What Tactyl Technologies, Inc. makes

Tactyl Technologies, Inc. manufactures powder-free and hypoallergenic examination gloves, surgical gloves, and lubricated condoms designed for medical and patient examination use. The gloves are intended for single-use in clinical, surgical, and examination settings to reduce allergic reactions and improve tactile sensitivity. Condoms are provided with lubrication for enhanced comfort and protection.

The company’s products are regulated under FDA’s Class I and Class II device classifications, with relevant submissions listed via the 510(k) pathway. These devices are intended for domestic and international markets, adhering to U.S. regulatory requirements. The company is headquartered in the United States.

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

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does Tactyl Technologies, Inc. have in the registry?

The registry currently lists 7 devices for Tactyl Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Tactyl Technologies, Inc.'s devices?

Among its 7 most recently registered devices, Tactyl Technologies, Inc. has devices listed in FDA 510(k) (7 devices).

What risk classes do Tactyl Technologies, Inc.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Tactyl Technologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Tactyl Technologies, Inc. in the registry?

The most recently registered devices listed for Tactyl Technologies, Inc. include TACTYLON POWDER FREE EXAMINATION GLOVE, POWDER FREE TACTYLON SURGEONS GLOVE, TACTYLON(TM) CONDOM and PATIENT EXAMINATION GLOVE/HYPOALLERGENIC.

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