Cameo, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Cameo, Inc. makes
Cameo, Inc. produces single-use medical trays for procedural preparation, including skin prep kits, amniocentesis trays, and basic biopsy trays. These trays are designed for sterile, disposable use in clinical settings to support diagnostic and procedural workflows.
The company’s products are classified under FDA’s Class I and Class II categories and are authorised via the 510(k) pathway. They are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Various Cameo Med Percutaneous Skin Prep Trays, Ref K922961
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Various Cameo Med Basic Biopsy Trays, Disposable Ref K922962
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cameo, Inc. have in the registry?
The registry currently lists 3 devices for Cameo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cameo, Inc.'s devices?
Among its 3 most recently registered devices, Cameo, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Cameo, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cameo, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cameo, Inc. in the registry?
The most recently registered devices listed for Cameo, Inc. include VARIOUS CAMEO MED PERCUTANEOUS SKIN PREP TRAYS,, VARIOUS CAMEO MED AMNIOCENTESIS TRAYS, DISPOSABLE and VARIOUS CAMEO MED BASIC BIOPSY TRAYS, DISPOSABLE.