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Sign in to claim this brandENDO-THERAPEUTICS, INC.
United States·US-MF-000002267
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 15251, Roosevelt Blvd, Clearwater, United States
- Website
- endotherapeutics.com
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Shawn Desrosiers
- EUDAMED SRN
- US-MF-000002267
- FDA FEI Number
- 1000132436
- DUNS Number
- —
Catalogue (159)
Page 3 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| BioCeps Biopsy Forceps, Laryngeal | ET1440 | FDA UDI | Class I | Unknown |
| EndoTNeedle | ET1320 | FDA UDI | Class II | Active |
| RotoNet | RT-NET-3-230-10 | FDA UDI | Class I | Active |
| BioCeps Biopsy Forceps | ET1430 | FDA UDI | Class I | Unknown |
| BioCeps Biopsy Forceps | ET1416 | FDA UDI | Class I | Unknown |
| RotoNet | RT-NET-3-350-5 | FDA UDI | Class I | Active |
| BioCeps Biopsy Forceps | ET1414 | FDA UDI | Class I | Unknown |
| EndoTGrasper | ET2021 | FDA UDI | Class II | Active |
| EndoTBasket | ET2033 | FDA UDI | Class II | Active |
| BioCeps Biopsy Forceps | ET1417 | FDA UDI | Class I | Unknown |
| Hexagonal Basket, Medium | BGH-1615M | FDA UDI | Class II | Unknown |
| Cytology Brush | CB-1615 | FDA UDI | Class II | Unknown |
| Biopsy Forceps - Hot | SG-111-615H | FDA UDI | Class II | Unknown |
| Biopsy Forceps - Hot | SG-211-622H | FDA UDI | Class II | Unknown |
| EndoTNeedle | ET1300 | EUDAMEDFDA UDI | Class II | Active |
| AcuJect Flex | AJ FLEX 25 230 10 | FDA UDI | Class II | Active |
| EndoTBasket | ET2030 | FDA UDI | Class II | Active |
| Cytology Brush | CB-1311 | FDA UDI | Class II | Unknown |
| Polypectomy Snare, Oval - Large | SGO-1622L | FDA UDI | Class II | Unknown |
| ezSnare Polypectomy Snare | ET1805 | FDA UDI | Class II | Active |
| Biopsy Forceps | SG-211-622 | FDA UDI | Class I | Unknown |
| BioCeps Biopsy Forceps | ET1400 | FDA UDI | Class II | Active |
| Biopsy Forceps - Hot | SG-211-615H | FDA UDI | Class II | Unknown |
| ezSnare Polypectomy Snare | ET1804 | FDA UDI | Class II | Unknown |
| Hexagonal Basket, Large | BGH-1622L | FDA UDI | Class II | Unknown |
| BioCeps Biopsy Forceps | ET1418 | FDA UDI | Class I | Unknown |
| Single Use Brush Biopsy Instrument | EGD-160-006 | EUDAMEDFDA UDI | Class I | Active |
| RotoNet | RT-NET-4-230-5 | FDA UDI | Class I | Active |
| EndoTGrasper | ET2022 | FDA UDI | Class II | Active |
| ezSnare Polypectomy Snare | ET1801 | FDA UDI | Class II | Active |
| ezSnare Polypectomy Snare | ET1814 | FDA UDI | Class II | Unknown |
| EndoTBrush Cytology Brush | ET1421 | EUDAMEDFDA UDI | Class II | Active |
| ezSnare Polypectomy Snare | ET1814 | FDA UDI | Class II | Active |
| BioCeps Biopsy Forceps | ET1410 | FDA UDI | Class II | Active |
| Tripod Grasper | GG-1615 | FDA UDI | Class II | Unknown |
| EndoTBasket | ET2041 | FDA UDI | Class II | Active |
| EndoTBasket | ET2042 | FDA UDI | Class II | Active |
| SwirlNet | ET2010 | EUDAMEDFDA UDI | Class I | Active |
| Endoport Erocar | K841716 | FDA 510(k) | Class II | Active |
| Mod. Endoport Single-Use Trocar And Sleeve | K860103 | FDA 510(k) | Class II | Active |
| Uroscan | K870855 | FDA 510(k) | Class II | Active |
| Endo-Glide Guidewire | K023603 | FDA 510(k) | Class II | Active |
| Multi-Bite Hot Biopsy Forceps | K090796 | FDA 510(k) | Class II | Active |
| Tissue Grasping Forceps, Scissors, Clamps And Dissectors For Laparoscopic Surgeries | K012725 | FDA 510(k) | Class II | Active |
| Endocath Electrophysiology Catheter | K926549 | FDA 510(k) | Class II | Active |
| Varices Injection Needle | K012977 | FDA 510(k) | Class II | Active |
| Endoport 5mm Single-Use Trocar And Sleeve | K860192 | FDA 510(k) | Class II | Active |
| Endoneedle | K844619 | FDA 510(k) | Class II | Active |
| Endoport 5mm | K852031 | FDA 510(k) | Class II | Active |
| Mod. Endoneedle Single-Use Pneumoperitoneum Needle | K860102 | FDA 510(k) | Class II | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Oct 24, 2022 | Z-0270-2023 | — | terminated | Improper device regulatory classification |