Percudisc, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Percudisc, Inc. makes
Percudisc, Inc. makes the Percudisc PLDD Delivery System/Procedure Kit and the Percudisc(TM) System, which are medical devices used for percutaneous laser disc decompression procedures.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Percudisc Pldd Delivery System/Procedure Kit Ref K920673
Regimes: 510(k) Registry: 510(k)Percudisc(Tm) System Ref K910823
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Percudisc, Inc. have in the registry?
The registry currently lists 2 devices for Percudisc, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Percudisc, Inc.'s devices?
Among its 2 most recently registered devices, Percudisc, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Percudisc, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Percudisc, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Percudisc, Inc. in the registry?
The most recently registered devices listed for Percudisc, Inc. include PERCUDISC PLDD DELIVERY SYSTEM/PROCEDURE KIT and PERCUDISC(TM) SYSTEM.