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Touch Scientific, Inc.

United StatesFDA applicant, unverified

Devices
3

What Touch Scientific, Inc. makes

Touch Scientific, Inc. manufactures diagnostic test kits and systems for detecting specific biomarkers in biological samples. The TOUCH Tear IGE Microassay Kit measures immunoglobulin E (IgE) levels in tear fluid, while the LactoCard and Lactoferrin Microassay System analyze lactoferrin concentrations, primarily for applications in ophthalmology and allergy diagnostics.

These products are regulated under FDA’s 510(k) pathway, with some classified as Class I and others as Class II devices. The company’s diagnostics are listed in the FDA’s 510(k) clearance registry, and the manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Touch Tear Ige Microassay Kit Ref K991316

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Lactocard Ref K931901

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Lactoferrin Microassay System Ref K934473

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

Frequently asked questions

How many devices does Touch Scientific, Inc. have in the registry?

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

Which registries list Touch Scientific, Inc.'s devices?

Among its 3 most recently registered devices, Touch Scientific, Inc. has devices listed in FDA 510(k) (3 devices).

What risk classes do Touch Scientific, Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Touch Scientific, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Touch Scientific, Inc. in the registry?

The most recently registered devices listed for Touch Scientific, Inc. include TOUCH TEAR IGE MICROASSAY KIT, LACTOCARD and LACTOFERRIN MICROASSAY SYSTEM.

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