Denver Biomaterials, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Denver Biomaterials, Inc. makes
Denver Biomaterials, Inc. makes Denver ascites shunts and percutaneous access kits, Denver PleurX pleural catheter kits and home drainage kits, Denver paracentesis needles with and without drainage lines and paracentesis trays, and Denver pleural effusion shunts with external pump chambers.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Denver Biomaterials, Inc. have in the registry?
The registry currently lists 4 devices for Denver Biomaterials, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Denver Biomaterials, Inc.'s devices?
Among its 4 most recently registered devices, Denver Biomaterials, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Denver Biomaterials, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Denver Biomaterials, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Denver Biomaterials, Inc. in the registry?
The most recently registered devices listed for Denver Biomaterials, Inc. include DENVER ASCITES SHUNTS, DENVER ASCITES SHUNT PERCUTANEOUS ACCESS KITS, DENVER PLEURX PLEURAL CATHETER KIT, CATALOG NO. 50-7000, DENVER PLEURX HOME DRAINAGE KIT, CATALOG NO. 50-7500, DENVER PARACENTESIS NEEDLE(60-1200) DENVER PARACENTESIS NEEDLE WITH DRAINAGE LINE(60-1100) DENVER PARACENTESIS TRAY and DENVER PLEURAL EFFUSION SHUNT WITH EXTERNAL PUMP CHAMBER.