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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 8 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | E424SR-45 | FDA UDI | Class II | Active |
| Endoplus | E343M | FDA UDI | Class II | Active |
| Endoplus | E338RR-45 | FDA UDI | Class II | Active |
| Endoplus | 10417 | FDA UDI | Class II | Active |
| Endoplus | E307MR | FDA UDI | Class II | Active |
| Endoplus | 5MRC-43L | FDA UDI | Class II | Active |
| Endoplus | E378MR | FDA UDI | Class II | Active |
| Endoplus | 5334 | FDA UDI | Class II | Active |
| Endoplus | E301S | FDA UDI | Class II | Active |
| Endoplus | 5XRRL | FDA UDI | Class II | Active |
| Endoplus | E414SR | FDA UDI | Class II | Active |
| Endoplus | E331MR | FDA UDI | Class II | Active |
| Endoplus | E346MR | FDA UDI | Class II | Active |
| Endoplus | E373MR-45 | FDA UDI | Class II | Active |
| Endoplus | 5325L | FDA UDI | Class II | Active |
| Endoplus | 5317 | FDA UDI | Class II | Active |
| Endoplus | E315M-45 | FDA UDI | Class II | Active |
| Endoplus | 5323 | FDA UDI | Class II | Active |
| Endoplus | 5322 | FDA UDI | Class II | Active |
| Endoplus | E313DVR-45 | FDA UDI | Class II | Active |
| Endoplus | 5365J | FDA UDI | Class II | Active |
| Endoplus | E412SLR | FDA UDI | Class II | Active |
| Endoplus | E317SR-45 | FDA UDI | Class II | Active |
| Endoplus | 317VL | FDA UDI | Class II | Active |
| Endoplus | 5370L | FDA UDI | Class II | Active |
| Endoplus | E420AC | FDA UDI | Class II | Active |
| Endoplus | E324SR | FDA UDI | Class II | Active |
| Endoplus | E390SLR-45 | FDA UDI | Class II | Active |
| Endoplus | E347MR-45 | FDA UDI | Class II | Active |
| Endoplus | 369VL | FDA UDI | Class II | Active |
| Endoplus | E369SR-37 | FDA UDI | Class II | Active |
| Endoplus | E346SL-37 | FDA UDI | Class II | Active |
| Endoplus | E377MR-45 | FDA UDI | Class II | Active |
| Endoplus | E402RR | FDA UDI | Class II | Active |
| Endoplus | 5310 | FDA UDI | Class II | Active |
| Endoplus | E377MR | FDA UDI | Class II | Active |
| Endoplus | 5357L | FDA UDI | Class II | Active |
| Endoplus | 5337J | FDA UDI | Class II | Active |
| Endoplus | E325S | FDA UDI | Class II | Active |
| Endoplus | E412SR | FDA UDI | Class II | Active |
| Endoplus | E337SR | FDA UDI | Class II | Active |
| Endoplus | EN704L | FDA UDI | Class II | Active |
| Endoplus | E432SLR | FDA UDI | Class II | Active |
| Endoplus | E309MR | FDA UDI | Class II | Active |
| Endoplus | 5368L | FDA UDI | Class II | Active |
| Endoplus | E332SLR | FDA UDI | Class II | Active |
| Endoplus | 5302L | FDA UDI | Class II | Active |
| Endoplus | 345VL | FDA UDI | Class II | Active |
| Endoplus | 5307 | FDA UDI | Class II | Active |
| Endoplus | 5390L | 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. |