Rudolph Beaver, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Rudolph Beaver, Inc. makes
Rudolph Beaver, Inc. makes surgical instruments including knives, cystitomes, gauge blocks, and arthroscopic tools such as the Beaver R-K Knife, Mechanical Cystitome, Beaver Micro-Gem Gauge Block, OCU-1, Arthro-Trac(TM), and Beaver Multipurpose Sapphire Knife.
The company's 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
Beaver R-K Knife Ref K852828
Regimes: 510(k) Registry: 510(k)Mechanical Cystitome Ref K862709
Regimes: 510(k) Registry: 510(k)Beaver Micro-Gem Gauge Block Ref K860305
Regimes: 510(k) Registry: 510(k)Ocu-1 Ref K875030
Regimes: 510(k) Registry: 510(k)Arthro-Trac(Tm) Ref K883361
Regimes: 510(k) Registry: 510(k)Beaver Multipurpose Sapphire Knife Ref K853129
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rudolph Beaver, Inc. have in the registry?
The registry currently lists 6 devices for Rudolph Beaver, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rudolph Beaver, Inc.'s devices?
Among its 6 most recently registered devices, Rudolph Beaver, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Rudolph Beaver, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Rudolph Beaver, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rudolph Beaver, Inc. in the registry?
The most recently registered devices listed for Rudolph Beaver, Inc. include BEAVER R-K KNIFE, MECHANICAL CYSTITOME, BEAVER MICRO-GEM GAUGE BLOCK and OCU-1.