Is this your brand? Sign in to claim ownership.
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 2 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ezSnare Polypectomy Snare | ET1803 | FDA UDI | Class II | Unknown |
| Single Use Brush Biopsy Instrument | WGB-200-006 | FDA UDI | Class I | Active |
| BioCeps Biopsy Forceps | ET1410 | FDA UDI | Class II | Unknown |
| EndoTGrasper | ET2020 | FDA UDI | Class II | Active |
| BioCeps Biopsy Forceps, Esophageal | ET1442 | FDA UDI | Class I | Unknown |
| Biopsy Forceps | SU-111-622 | FDA UDI | Class I | Unknown |
| BioCeps Biopsy Forceps | ET1418 | FDA UDI | Class I | Active |
| ezSnare Polypectomy Snare | ET1807 | FDA UDI | Class II | Active |
| EndoTBasket | ET2034 | FDA UDI | Class II | Active |
| Catchem' Polyp Trap | ET2212 | FDA UDI | Class II | Unknown |
| Biopsy Brush | LBB-95 | FDA UDI | Class I | Active |
| EndoTBasket | ET2032 | FDA UDI | Class II | Active |
| Hexagonal Basket, Medium | BGH-1622M | FDA UDI | Class II | Unknown |
| BioCeps Biopsy Forceps | ET1412 | FDA UDI | Class I | Unknown |
| ezSnare Polypectomy Snare | ET1801 | FDA UDI | Class II | Unknown |
| BioCeps Biopsy Forceps | ET1417 | FDA UDI | Class I | Active |
| Polypectomy Snare, Oval-Large | SGO-1315L | FDA UDI | Class II | Unknown |
| Biopsy Forceps | SU-211-615 | FDA UDI | Class I | Unknown |
| ezSnare Polypectomy Snare | ET1806 | FDA UDI | Class II | Active |
| RotoNet | RT-NET-2-160-5 | FDA UDI | Class I | Active |
| EndoTNeedle | ET1321 | FDA UDI | Class II | Active |
| ezSnare Polypectomy Snare | ET1805 | FDA UDI | Class II | Unknown |
| BioCeps Biopsy Forceps | ET1402 | FDA UDI | Class II | Unknown |
| Elliptical Basket, Large | BGE-1622L | FDA UDI | Class II | Unknown |
| AcuJect Flex | AJ FLEX 23 230 10 | FDA UDI | Class II | Active |
| Elliptical Basket, Large | BGE-1615L | FDA UDI | Class II | Unknown |
| Endoscopic injection needle | SN-1623-22 | FDA UDI | Class II | Unknown |
| Tripod Grasper | GG-1622 | FDA UDI | Class II | Unknown |
| eSuction | ET2001 | EUDAMEDFDA UDI | Class I | Active |
| BioCeps Biopsy Forceps | ET1413 | FDA UDI | Class I | Active |
| BioCeps Biopsy Forceps, Laryngeal | ET1440 | FDA UDI | Class I | Active |
| BioCeps Biopsy Forceps | ET1414 | FDA UDI | Class I | Active |
| 4 Chamber Polyp Trap | AT-PT-4-12 | FDA UDI | Class II | Active |
| BioCeps Biopsy Forceps | ET1415 | FDA UDI | Class I | Unknown |
| Biopsy Forceps | SG-111-622 | FDA UDI | Class I | Unknown |
| ezSnare Polypectomy Snare | ET1800 | FDA UDI | Class II | Active |
| Polypectomy Snare, Oval - Small | SGO-1315S | FDA UDI | Class II | Unknown |
| ezSnare Polypectomy Snare | ET1807 | FDA UDI | Class II | Unknown |
| ezSnare Polypectomy Snare | ET1802 | FDA UDI | Class II | Unknown |
| BioCeps Biopsy Forceps | ET1413 | FDA UDI | Class I | Unknown |
| ezSnare Polypectomy Snare | ET1806 | FDA UDI | Class II | Unknown |
| EndoTBasket | ET2046 | FDA UDI | Class II | Active |
| BioCeps Biopsy Forceps | ET1419 | FDA UDI | Class I | Unknown |
| Polypectomy Snare, Oval - Medium | SGO-1315M | FDA UDI | Class II | Unknown |
| Biopsy Forceps | SG-111-612 | FDA UDI | Class I | Unknown |
| BioCeps Biopsy Forceps | ET1411 | FDA UDI | Class II | Unknown |
| RotoNet | RT-NET-4-160-5 | FDA UDI | Class I | Active |
| RotoNet | RT-NET-3-160-5 | FDA UDI | Class I | Active |
| Biopsy Forceps | SG-211-615 | FDA UDI | Class I | Unknown |
| EndoTBasket | ET2043 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
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 |