Oska, Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000054811 FEI 3012833018
- Devices
- 1
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Oska Pulse Ref MD4001/OP9003
Regimes: CE MDD Registry: EUDAMED
Company details
- EUDAMED SRN
- US-MF-000054811
- FDA FEI number
- 3012833018
- EUDAMED status
- Active
- EUDAMED registered name
- Oska, Inc.
- EUDAMED abbreviated name
- Oska
- Registered address
- 2725, Jefferson Street, 92008, Carlsbad, United States
- Website
- www.oskawellness.com
- facebook.com/oskawellness
- [email protected]
- Phone
- +1 844 630 9932
- PRRC contact
- Chip Currey
From the company website
Oska Pulse works at the source of pain to decrease inflammation, increase circulation, improve mobility and relieve pain. Oska Pulse is a medical pain relief device that uses Pulsed Electromagnetic Fields (PEMF) to relieve pain at the source.
Frequently asked questions
How many devices does Oska, Inc. have in the registry?
The registry currently lists 1 device for Oska, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oska, Inc.'s devices?
Among its 1 most recently registered device, Oska, Inc. has devices listed in EUDAMED (1 device).
What risk classes do Oska, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Oska, Inc.'s devices are Class IIa. Each device page shows its own class and authorisation.
What are the newest devices from Oska, Inc. in the registry?
The most recently registered devices listed for Oska, Inc. include Oska Pulse.