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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 18 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | E348SLR | FDA UDI | Class II | Active |
| Endoplus | ES8500-45SLR | FDA UDI | Class II | Active |
| Endoplus | E355RR | FDA UDI | Class II | Active |
| Endoplus | 10420L | FDA UDI | Class II | Active |
| Endoplus | E327MR-45 | FDA UDI | Class II | Active |
| Endoplus | E336SR | FDA UDI | Class II | Active |
| Endoplus | E369SR | FDA UDI | Class II | Active |
| Endoplus | E321RR | FDA UDI | Class II | Active |
| Endoplus | E355M | FDA UDI | Class II | Active |
| Endoplus | E311MR-45 | FDA UDI | Class II | Active |
| Endoplus | 10446L | FDA UDI | Class II | Active |
| Endoplus | 5318L | FDA UDI | Class II | Active |
| Endoplus | E375SR | FDA UDI | Class II | Active |
| Endoplus | su5850L | FDA UDI | Class II | Active |
| Endoplus | E304SR-45 | FDA UDI | Class II | Active |
| Endoplus | 5SLRN | FDA UDI | Class II | Active |
| Endoplus | E327ACR | FDA UDI | Class II | Active |
| Endoplus | E312MR-25 | FDA UDI | Class II | Active |
| Endoplus | E331DVR | FDA UDI | Class II | Active |
| Endoplus | E341RR-45 | FDA UDI | Class II | Active |
| Endoplus | E349SLR | FDA UDI | Class II | Active |
| Endoplus | 5346 | FDA UDI | Class II | Active |
| Endoplus | 346VL | FDA UDI | Class II | Active |
| Endoplus | 5314L | FDA UDI | Class II | Active |
| Endoplus | E424ACR | FDA UDI | Class II | Active |
| Endoplus | EN306 | FDA UDI | Class II | Active |
| Endoplus | E372MR-45 | FDA UDI | Class II | Active |
| Endoplus | E313SLR | FDA UDI | Class II | Active |
| Endoplus | E424SR | FDA UDI | Class II | Active |
| Endoplus | E345SL | FDA UDI | Class II | Active |
| Endoplus | E301SLR | FDA UDI | Class II | Active |
| Endoplus | E434SR | FDA UDI | Class II | Active |
| Endoplus | E308MR-25 | FDA UDI | Class II | Active |
| Endoplus | E311M | FDA UDI | Class II | Active |
| Endoplus | 5315 | FDA UDI | Class II | Active |
| Endoplus | E307SLR | FDA UDI | Class II | Active |
| Endoplus | E312AC | FDA UDI | Class II | Active |
| Endoplus | 5308L | FDA UDI | Class II | Active |
| Endoplus | E300SR | FDA UDI | Class II | Active |
| Endoplus | E347R | FDA UDI | Class II | Active |
| Endoplus | 5350 | FDA UDI | Class II | Active |
| Endoplus | 5331 | FDA UDI | Class II | Active |
| Endoplus | E334MR | FDA UDI | Class II | Active |
| Endoplus | E346ACR | FDA UDI | Class II | Active |
| Endoplus | E330SLR-45 | FDA UDI | Class II | Active |
| Endoplus | E369RR-37 | FDA UDI | Class II | Active |
| Endoplus | E364SR-45 | FDA UDI | Class II | Active |
| Endoplus | 5365L | FDA UDI | Class II | Active |
| Endoplus | E424AC-45 | FDA UDI | Class II | Active |
| Endoplus | 5RS | 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. |