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American Instrument Manufacturer'S, Inc.

United StatesFDA applicant, unverified

Devices
2

What American Instrument Manufacturer'S, Inc. makes

American Instrument Manufacturer’s, Inc. produces surgical cannulas designed for plastic surgery procedures, including the L-5 series, as well as the ULS 8-86 device, which appears to be a specialized surgical instrument.

These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Uls 8-86 Ref K863163

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • L-5 Plastic Surgery Cannulas Ref K880669

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

Frequently asked questions

How many devices does American Instrument Manufacturer'S, Inc. have in the registry?

The registry currently lists 2 devices for American Instrument Manufacturer'S, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list American Instrument Manufacturer'S, Inc.'s devices?

Among its 2 most recently registered devices, American Instrument Manufacturer'S, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do American Instrument Manufacturer'S, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for American Instrument Manufacturer'S, Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from American Instrument Manufacturer'S, Inc. in the registry?

The most recently registered devices listed for American Instrument Manufacturer'S, Inc. include ULS 8-86 and L-5 PLASTIC SURGERY CANNULAS.

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