Protaryx Medical, Inc.
United Statesfrom the FDA registration address FDA FEI 3046772394
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Protaryx Medical, Inc. makes
Protaryx Medical, Inc. manufactures the Protaryx Transseptal Puncture Device (PTX2-001), a tool designed for transseptal puncture procedures in cardiac interventions.
The company’s device portfolio is regulated under FDA Class II and is listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
Protaryx Transseptal Puncture Device (PTX2-001) Ref K260839
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3046772394
- DUNS number
- 111966427
- Address
- 323 W Camden St Ste 600, Baltimore, MD, 21201
- [email protected]
- Phone
- 1-512-554-9628
Frequently asked questions
How many devices does Protaryx Medical, Inc. have in the registry?
The registry currently lists 2 devices for Protaryx Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Protaryx Medical, Inc.'s devices?
Among its 2 most recently registered devices, Protaryx Medical, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Protaryx Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Protaryx Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Protaryx Medical, Inc. in the registry?
The most recently registered devices listed for Protaryx Medical, Inc. include Transseptal Puncture Device PTX2-001 and Protaryx Transseptal Puncture Device (PTX2-001).