Polyclinic Medical Center
Country not established
- Devices
- 2
What Polyclinic Medical Center makes
Polyclinic Medical Center manufactures the SCHULTZ ENDHOLD, a device designed for endoscopic procedures, and the HARD TISSUE REPLACE (HTR)-PATIENT-MATCH IMPLANT, a custom-fitted implant for tissue replacement applications.
The company’s portfolio includes Class I and Class II devices, all of which are listed via the FDA’s 510(k) pathway. These products are regulated under US medical device laws and are based in the United States.
Catalogue
Schultz Endhold Ref K833332
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Polyclinic Medical Center have in the registry?
The registry currently lists 2 devices for Polyclinic Medical Center. Devices recorded under merged duplicate company entries are counted once.
Which registries list Polyclinic Medical Center's devices?
Among its 2 most recently registered devices, Polyclinic Medical Center has devices listed in FDA 510(k) (2 devices).
What risk classes do Polyclinic Medical Center's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Polyclinic Medical Center's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Polyclinic Medical Center in the registry?
The most recently registered devices listed for Polyclinic Medical Center include SCHULTZ ENDHOLD and HARD TISSUE REPLACE(HTR(R))-PATIENT-MATCH IMPLANT.