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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 6 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | 5338 | FDA UDI | Class II | Active |
| Endoplus | 5316 | FDA UDI | Class II | Active |
| Endoplus | su5850J | FDA UDI | Class II | Active |
| Endoplus | E345SLR | FDA UDI | Class II | Active |
| Endoplus | 5MRS | FDA UDI | Class II | Active |
| Endoplus | E369MR | FDA UDI | Class II | Active |
| Endoplus | E365MR | FDA UDI | Class II | Active |
| Endoplus | 5398L | FDA UDI | Class II | Active |
| Endoplus | 5MRR | FDA UDI | Class II | Active |
| Endoplus | 5311L | FDA UDI | Class II | Active |
| Endoplus | E325RR | FDA UDI | Class II | Active |
| Endoplus | E364R-45 | FDA UDI | Class II | Active |
| Endoplus | 5367L | FDA UDI | Class II | Active |
| Endoplus | E318M | FDA UDI | Class II | Active |
| Endoplus | E317M | FDA UDI | Class II | Active |
| Endoplus | E333MR-25 | FDA UDI | Class II | Active |
| Endoplus | E333SR | FDA UDI | Class II | Active |
| Endoplus | E347M-45 | FDA UDI | Class II | Active |
| Endoplus | E340SR | FDA UDI | Class II | Active |
| Endoplus | 5348 | FDA UDI | Class II | Active |
| Endoplus | E325SLR | FDA UDI | Class II | Active |
| Endoplus | 5363L | FDA UDI | Class II | Active |
| Endoplus | E369RR | FDA UDI | Class II | Active |
| Endoplus | E331SR | FDA UDI | Class II | Active |
| Endoplus | 5RFR | FDA UDI | Class II | Active |
| Endoplus | E322AC-45 | FDA UDI | Class II | Active |
| Endoplus | E341DVR | FDA UDI | Class II | Active |
| Endoplus | E308M | FDA UDI | Class II | Active |
| Endoplus | E369S-45 | FDA UDI | Class II | Active |
| Endoplus | E322AC | FDA UDI | Class II | Active |
| Endoplus | E369SLR | FDA UDI | Class II | Active |
| Endoplus | 5326L | FDA UDI | Class II | Active |
| Endoplus | E304RR-38 | FDA UDI | Class II | Active |
| Endoplus | E341SR | FDA UDI | Class II | Active |
| Endoplus | 336VA | FDA UDI | Class II | Active |
| Endoplus | 323VA | FDA UDI | Class II | Active |
| Endoplus | E420S | FDA UDI | Class II | Active |
| Endoplus | E332M | FDA UDI | Class II | Active |
| Endoplus | E302SR | FDA UDI | Class II | Active |
| Endoplus | E325RR-45 | FDA UDI | Class II | Active |
| Endoplus | 5372 | FDA UDI | Class II | Active |
| Endoplus | E312SR | FDA UDI | Class II | Active |
| Endoplus | E327RR | FDA UDI | Class II | Active |
| Endoplus | E309SR | FDA UDI | Class II | Active |
| Endoplus | E341SLR-45 | FDA UDI | Class II | Active |
| Endoplus | E310RR | FDA UDI | Class II | Active |
| Endoplus | E434SLR | FDA UDI | Class II | Active |
| Endoplus | E327DVR-45 | FDA UDI | Class II | Active |
| Endoplus | EN310 | FDA UDI | Class II | Active |
| Endoplus | E364AC-45 | 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. |