Pdo Max
Also registered as Pdo Max, Inc.
Country not established FDA establishment FEI 3015289316
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
PDO Max Suture with Dual Needle Ref K210871
510(k) 510(k)PDS Barbed Suture, PDO MAXX Threads Ref K190245
510(k) 510(k)
Company details
- FDA FEI number
- 3015289316
- Address
- 4971 Bear Road, Liverpool, NY, 13088
Frequently asked questions
How many devices does PDO MAX have in the registry?
The registry currently lists 2 devices for PDO MAX. Devices recorded under merged duplicate company entries are counted once.
Which registries list PDO MAX's devices?
Among its 2 most recently registered devices, PDO MAX has devices listed in FDA 510(k) (2 devices).
What risk classes do PDO MAX's devices fall under?
Among its 2 most recently registered devices, the classes recorded for PDO MAX's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PDO MAX in the registry?
The most recently registered devices listed for PDO MAX include PDO Max Suture with Dual Needle and PDS Barbed Suture, PDO MAXX Threads.