Porges Corp.
Le Plessis Robinson Cedex, FR
Porges Corp. appears in FDA device records in Le Plessis Robinson Cedex, FR. FDA records list 22 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 22
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 22 510(k) clearances for Porges Corp. between 1988 and 2002. The busiest year on record is 1990, with 13. The most recent is 2002, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 2 |
| 1989 | 3 |
| 1990 | 13 |
| 2001 | 1 |
| 2002 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K021856 | PORGES URETERAL CATHETERS, MODELS ACN6XX, ACN5XX, AC5B, AC5C07, ACP5XX, ACP2XX, ACP3XX, ACP4XX, ACP6XX | EYB | Substantially Equivalent | |
| K013921 | PORGES SILICONE DOUBLE LOOP URETERAL STENT, MODEL # AJ4X / BJ1X / BJ2X | FAD | Substantially Equivalent | |
| K013174 | PROGES FOLYSIL SILICONE FOLEY CATHETER, STRAIGHT CYLINDRICAL TIP, SILICONE FEMALE FOLEY CATHETER, STRAIGHT CYLINDRICAL, | EZL | Substantially Equivalent | |
| K013172 | PORGES SILICONE PROSTATECTOMY CATHETER, STRAIGHT CYLINDRICAL TIP, DELINOTTE TIP, DUFOUR TIP, OVER THE GUIDE TIP, MODEL | EZL | Substantially Equivalent | |
| K900269 | PORGES DORMIA 3 FR FLAT WIRE BASKET STONE DISLODGE | FFL | Substantially Equivalent | |
| K900031 | MODIFIED PEDIATRIC SILICONE FOLEY CATHETERS | KNY | Substantially Equivalent | |
| K896505 | PORGES UNIVERSAL HANDLES | GCP | Substantially Equivalent | |
| K896503 | PORGES ERCP CATHETERS | FGE | Substantially Equivalent | |
| K896507 | PORGES DIATHERMY SNARE | KNS | Substantially Equivalent | |
| K896425 | PORGES CYTOLOGY BRUSHES | FDX | Substantially Equivalent | |
| K896506 | PORGES ENDOSCOPIC DORMIA EXTRACTORS, DORMIATRIPTOR | FGE | Substantially Equivalent | |
| K896504 | PORGES 2-WAY BALLOON EXTRACTION CATHETER | FGE | Substantially Equivalent | |
| K896424 | PORGES SCLEROTHERAPY NEEDLES | FBK | Substantially Equivalent | |
| K896502 | PORGES BIOPSY & FOREIGN BODY FORCEPS | OCZ | Substantially Equivalent | |
| K896426 | PORGES SPHINCTEROTOMES | KNS | Substantially Equivalent | |
| K896423 | PORGES BILIARY STENTS | FGE | Substantially Equivalent | |
| K896376 | PORGES NASOBILIARY DRAIN | FGE | Substantially Equivalent | |
| K896537 | PORGES HOT BIOPSY FORCEPS | KGE | Substantially Equivalent | |
| K892384 | BILIARY ENDOPROSTHESIS AND EXTERNAL CATHETER | FGE | Substantially Equivalent | |
| K892383 | BILIARY ENDOPROSTHESIS FOR INTERNAL DRAINAGE SET | FGE | Substantially Equivalent | |
| K883526 | PORGES STEPPED NEOPLEX DILATOR | KNQ | Substantially Equivalent | |
| K881097 | SPEC 5* SUPRAPUBIC CATHETER | KOB | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KNYAccessories, Catheter, G-U
- EZLCatheter, Retention Type, Balloon
- KOBCatheter, Suprapubic (And Accessories)
- EYBCatheter, Ureteral, Gastro-Urology
- KNQDilator, Esophageal
- FFLDislodger, Stone, Basket, Ureteral, Metal
- GCPEndoscope, Ac-Powered And Accessories
- FDXEndoscopic Cytology Brush
- OCZEndoscopic Grasping/Cutting Instrument, Non-Powered
- FBKEndoscopic Injection Needle, Gastroenterology-Urology
- KGEForceps, Biopsy, Electric
- FADStent, Ureteral
- FGEStents, Drains And Dilators For The Biliary Ducts
- KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain