Peleton Surgical
United Statesfrom the FDA registration address FDA FEI 3019932374
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3019932374
- Address
- 1435 North Hayden Road, Suite 100, Scottsdale, AZ, 85257
Frequently asked questions
How many devices does Peleton Surgical have in the registry?
The registry currently lists 1 device for Peleton Surgical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Peleton Surgical's devices?
Among its 1 most recently registered device, Peleton Surgical has devices listed in FDA 510(k) (1 device).
What risk classes do Peleton Surgical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Peleton Surgical's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Peleton Surgical in the registry?
The most recently registered devices listed for Peleton Surgical include Peleton Universal Single Use Power System and Attachments.