Company ยท US
Endo-Therapeutics, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1993 to 2009. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| DRF | Catheter, Electrode Recording, Or Probe, Electrode Recording | 1 |
| FBK | Endoscopic Injection Needle, Gastroenterology-Urology | 1 |
| FCL | Forceps, Biopsy, Non-Electric | 1 |
| FGX | Snare, Non-Electrical | 1 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 1 |
| KGE | Forceps, Biopsy, Electric | 1 |
| KNS | Unit, Electrosurgical, Endoscopic (With Or Without Accessories) | 1 |
| OCY | Endoscopic Guidewire, Gastroenterology-Urology | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 25, 2009 | K090796 | MULTI-BITE HOT BIOPSY FORCEPS Endo-Therapeutics, Inc. | KGE |
| Jun 27, 2003 | K031026 | ETI BIPOLAR HEMOSTATIC PROBE Endo-Therapeutics, Inc. | KNS |
| Feb 19, 2003 | K023603 | ENDO-GLIDE GUIDEWIRE Endo-Therapeutics, Inc. | OCY |
| Nov 8, 2001 | K012725 | TISSUE GRASPING FORCEPS, SCISSORS, CLAMPS AND DISSECTORS FOR LAPAROSCOPIC SURGERIES Endo-Therapeutics, Inc. | GEI |
| Nov 2, 2001 | K012977 | VARICES INJECTION NEEDLE Endo-Therapeutics, Inc. | FBK |
| Dec 6, 1993 | K926549 | ENDOCATH ELECTROPHYSIOLOGY CATHETER Endo-Therapeutics, Inc. | DRF |
| Nov 5, 1993 | K925392 | BIOPSY FORCEPS Endo-Therapeutics, Inc. | FCL |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 18, 2022 | Endo-Therapeutics, Inc. eSuction Small Cavity, Model ET2005 Terminated |
FGX | None listed |