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Sign in to claim this brandEndoplus
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 750 Tower Rd Ste A, Mundelein, IL, 60060
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3000719482
- DUNS Number
- 794679167
Catalogue (902)
Page 9 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | E327DVR | FDA UDI | Class II | Active |
| Endoplus | EN801L | FDA UDI | Class II | Active |
| Richard Wolf | 8383.2925 | FDA UDI | Class II | Active |
| Endoplus | E310MR | FDA UDI | Class II | Active |
| Endoplus | 5341L | FDA UDI | Class II | Active |
| Endoplus | E377AC-45 | FDA UDI | Class II | Active |
| Endoplus | E346SR-45 | FDA UDI | Class II | Active |
| Endoplus | E319RR | FDA UDI | Class II | Active |
| Endoplus | E333DVR-45 | FDA UDI | Class II | Active |
| Endoplus | 5305L | FDA UDI | Class II | Active |
| Endoplus | E365MR-25 | FDA UDI | Class II | Active |
| Endoplus | E364MR | FDA UDI | Class II | Active |
| Endoplus | E303RR | FDA UDI | Class II | Active |
| Endoplus | 5323L | FDA UDI | Class II | Active |
| Endoplus | E341MR-45 | FDA UDI | Class II | Active |
| Endoplus | E325MR-45 | FDA UDI | Class II | Active |
| Endoplus | 10RRL | FDA UDI | Class II | Active |
| Endoplus | E382RR | FDA UDI | Class II | Active |
| Endoplus | E330SR | FDA UDI | Class II | Active |
| Endoplus | 10424 | FDA UDI | Class II | Active |
| Endoplus | 10412L | FDA UDI | Class II | Active |
| Endoplus | E424RR | FDA UDI | Class II | Active |
| Endoplus | 5651L | FDA UDI | Class II | Active |
| Endoplus | E341DVR-45 | FDA UDI | Class II | Active |
| Endoplus | 5312 | FDA UDI | Class II | Active |
| Endoplus | E365MR-32 | FDA UDI | Class II | Active |
| Endoplus | 5651 | FDA UDI | Class II | Active |
| Endoplus | E346RR-45 | FDA UDI | Class II | Active |
| Endoplus | E324ACR | FDA UDI | Class II | Active |
| Endoplus | 5750 | FDA UDI | Class II | Active |
| Endoplus | su5652 | FDA UDI | Class II | Active |
| Endoplus | E347DVR | FDA UDI | Class II | Active |
| Endoplus | E347RR-45 | FDA UDI | Class II | Active |
| Endoplus | E332SR | FDA UDI | Class II | Active |
| Endoplus | 5369L | FDA UDI | Class II | Active |
| Endoplus | E320MR | FDA UDI | Class II | Active |
| Endoplus | su5651L | FDA UDI | Class II | Active |
| Endoplus | 5318 | FDA UDI | Class II | Active |
| Endoplus | 5309 | FDA UDI | Class II | Active |
| Endoplus | E431RR | FDA UDI | Class II | Active |
| Endoplus | E364RR | FDA UDI | Class II | Active |
| Endoplus | 10446 | FDA UDI | Class II | Active |
| Endoplus | E382SR | FDA UDI | Class II | Active |
| Endoplus | E333DVR | FDA UDI | Class II | Active |
| Endoplus | E420DVR-45 | FDA UDI | Class II | Active |
| Endoplus | EN805 | FDA UDI | Class II | Active |
| Endoplus | 5343L | FDA UDI | Class II | Active |
| Endoplus | E347S | FDA UDI | Class II | Active |
| Endoplus | 5381 | FDA UDI | Class II | Active |
| Endoplus | 5328 | FDA UDI | Class II | Active |
Related Companies
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Authorities
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FDA Recalls (2)
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 |
|---|---|---|---|---|
| Jul 15, 2013 | Z-2265-2013 | — | terminated | Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures. |
| Jul 15, 2013 | Z-2264-2013 | — | terminated | Multiple complaints reporting that the moveable jaw has broken during laparoscopic procedures. |