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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 2 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | E364MR-45 | FDA UDI | Class II | Active |
| Endoplus | 10404L | FDA UDI | Class II | Active |
| Endoplus | E337SR-45 | FDA UDI | Class II | Active |
| Endoplus | E380AC | FDA UDI | Class II | Active |
| Endoplus | E330MR-37 | FDA UDI | Class II | Active |
| Endoplus | E329SLR | FDA UDI | Class II | Active |
| Endoplus | 5380 | FDA UDI | Class II | Active |
| Endoplus | E333MR | FDA UDI | Class II | Active |
| Endoplus | E381RR | FDA UDI | Class II | Active |
| Endoplus | 5FRL | FDA UDI | Class II | Active |
| Endoplus | E334AC | FDA UDI | Class II | Active |
| Endoplus | E323MR | FDA UDI | Class II | Active |
| Endoplus | E365RR | FDA UDI | Class II | Active |
| Endoplus | 5377 | FDA UDI | Class II | Active |
| Endoplus | E300R | FDA UDI | Class II | Active |
| Endoplus | 5XRL | FDA UDI | Class II | Active |
| Endoplus | E424S | FDA UDI | Class II | Active |
| Endoplus | 5362L | FDA UDI | Class II | Active |
| Endoplus | 5RL | FDA UDI | Class II | Active |
| Endoplus | E330R | FDA UDI | Class II | Active |
| Endoplus | E330MR | FDA UDI | Class II | Active |
| Endoplus | 365VL | FDA UDI | Class II | Active |
| Endoplus | 5MRRL | FDA UDI | Class II | Active |
| Endoplus | 10MRR | FDA UDI | Class II | Active |
| Endoplus | 5366 | FDA UDI | Class II | Active |
| Endoplus | E336SLR-32 | FDA UDI | Class II | Active |
| Endoplus | E321MR | FDA UDI | Class II | Active |
| Endoplus | E304S | FDA UDI | Class II | Active |
| Endoplus | 5307L | FDA UDI | Class II | Active |
| Endoplus | EN802 | FDA UDI | Class II | Active |
| Richard Wolf | 8383.2935 | FDA UDI | Class II | Active |
| Endoplus | E343MR-45 | FDA UDI | Class II | Active |
| Endoplus | EN304 | FDA UDI | Class II | Active |
| Endoplus | 5397L | FDA UDI | Class II | Active |
| Endoplus | EN309 | FDA UDI | Class II | Active |
| Endoplus | 5554 | FDA UDI | Class II | Active |
| Endoplus | E390SR | FDA UDI | Class II | Active |
| Endoplus | E332R | FDA UDI | Class II | Active |
| Endoplus | E396DVR | FDA UDI | Class II | Active |
| Endoplus | E302SLR-45 | FDA UDI | Class II | Active |
| Endoplus | 53978J | FDA UDI | Class II | Active |
| Endoplus | E381SLR | FDA UDI | Class II | Active |
| Endoplus | 325VA | FDA UDI | Class II | Active |
| Endoplus | E333ACR | FDA UDI | Class II | Active |
| Endoplus | E431R | FDA UDI | Class II | Active |
| Endoplus | 5XR | FDA UDI | Class II | Active |
| Endoplus | su5650J | FDA UDI | Class II | Active |
| Endoplus | 5324 | FDA UDI | Class II | Active |
| Endoplus | 5339L | FDA UDI | Class II | Active |
| Endoplus | 5368 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
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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. |