Porges S.A.
FranceFDA applicant, unverified
- Devices
- 4
What Porges S.A. makes
Porges S.A. manufactures silicone ureteral stents, ureteral catheters, Foley catheters, and prostatectomy catheters with various tip configurations including straight cylindrical, Delinotte, Dufour, and over-the-guide designs.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Porges Ureteral Catheters, Models ACN6XX, ACN5XX, AC5B, AC5C07, ACP5XX, ACP2XX, ACP3XX, ACP4XX, ACP6XX Ref K021856
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Porges S.A. have in the registry?
The registry currently lists 4 devices for Porges S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Porges S.A.'s devices?
Among its 4 most recently registered devices, Porges S.A. has devices listed in FDA 510(k) (4 devices).
What risk classes do Porges S.A.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Porges S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Porges S.A. in the registry?
The most recently registered devices listed for Porges S.A. include PORGES SILICONE DOUBLE LOOP URETERAL STENT, MODEL # AJ4X / BJ1X / BJ2X, PORGES URETERAL CATHETERS, MODELS ACN6XX, ACN5XX, AC5B, AC5C07, ACP5XX, ACP2XX, ACP3XX, ACP4XX, ACP6XX, PROGES FOLYSIL SILICONE FOLEY CATHETER, STRAIGHT CYLINDRICAL TIP, SILICONE FEMALE FOLEY CATHETER, STRAIGHT CYLINDRICAL, and PORGES SILICONE PROSTATECTOMY CATHETER, STRAIGHT CYLINDRICAL TIP, DELINOTTE TIP, DUFOUR TIP, OVER THE GUIDE TIP, MODEL.