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Opportunity, Inc.

United StatesFDA applicant, unverified

Devices
8

What Opportunity, Inc. makes

Opportunity, Inc. manufactures single-use surgical and procedural trays, including bone marrow biopsy and aspiration sets, incision and drainage trays, laceration repair kits, tracheostomy care kits, intravenous start kits, suture removal kits, and general-purpose surgical trays. These products are designed for sterile use in outpatient and procedural settings to support wound care, minor surgery, and diagnostic procedures.

The company’s devices are regulated under FDA’s Class I, Class II, and Unclassified (U) categories, with most cleared via the 510(k) pathway. Products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.

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

Catalogue8

Newest first, rows 1-8 of 8

Frequently asked questions

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

The registry currently lists 8 devices for Opportunity, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Opportunity, Inc.'s devices?

Among its 8 most recently registered devices, Opportunity, Inc. has devices listed in FDA 510(k) (8 devices).

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

Among its 8 most recently registered devices, the classes recorded for Opportunity, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Opportunity, Inc. include OPPORTUNITY INC. BONE MARROW BIOPSY AND ASPIRATION TRAY, OPPORTUNITY DRESSING CHANGE TRAY, OPPORTUNITY INCISION AND DRAINAGE TRAY and OPPORTUNITY, INC. LACERATION TRAY.

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