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Glederer & Co., Inc.

United StatesFDA applicant, unverified

Devices
2

What Glederer & Co., Inc. makes

Glederer & Co., Inc. manufactures the ACU-HALT, a device designed for acute pain management, and the ACU-LAB, a laboratory tool for analyzing or processing biological samples, likely related to medical diagnostics or research.

The company’s portfolio is regulated under the FDA’s 510(k) clearance process, indicating these devices fall under Class II risk classification. Both devices are listed in the FDA’s 510(k) 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.

Catalogue2

Newest first, rows 1-2 of 2

  • Acu-Halt Ref K955661

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Acu-Lab Ref K955776

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

Frequently asked questions

How many devices does Glederer & Co., Inc. have in the registry?

The registry currently lists 2 devices for Glederer & Co., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Glederer & Co., Inc.'s devices?

Among its 2 most recently registered devices, Glederer & Co., Inc. has devices listed in FDA 510(k) (2 devices).

What are the newest devices from Glederer & Co., Inc. in the registry?

The most recently registered devices listed for Glederer & Co., Inc. include ACU-HALT and ACU-LAB.

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