Occam Design
United Statesfrom the FDA registration address FDA FEI 3008657524
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Occam Design makes
Occam Design manufactures the OUCHLESS Model PN10114, a Class I medical device designed for a specific non-invasive procedure or application (device category unspecified).
The OUCHLESS Model PN10114 is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ouchless Model PN10114 Ref K093951
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3008657524
- Address
- 1044 East Chestnuts St, Louisville, KY, 40204
Frequently asked questions
How many devices does Occam Design have in the registry?
The registry currently lists 1 device for Occam Design. Devices recorded under merged duplicate company entries are counted once.
Which registries list Occam Design's devices?
Among its 1 most recently registered device, Occam Design has devices listed in FDA 510(k) (1 device).
What are the newest devices from Occam Design in the registry?
The most recently registered devices listed for Occam Design include OUCHLESS MODEL PN10114.