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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 1 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | 5375 | FDA UDI | Class II | Active |
| Endoplus | E328MR | FDA UDI | Class II | Active |
| Endoplus | E308RR-45 | FDA UDI | Class II | Active |
| Endoplus | E377RR | FDA UDI | Class II | Active |
| Endoplus | E333RR-37 | FDA UDI | Class II | Active |
| Endoplus | 5552 | FDA UDI | Class II | Active |
| Endoplus | 5SLR | FDA UDI | Class II | Active |
| Endoplus | 5150L | FDA UDI | Class II | Active |
| Endoplus | 5321L | FDA UDI | Class II | Active |
| Endoplus | E373MR | FDA UDI | Class II | Active |
| Endoplus | E313MR | FDA UDI | Class II | Active |
| Endoplus | 5363 | FDA UDI | Class II | Active |
| Endoplus | 336VL | FDA UDI | Class II | Active |
| Endoplus | E434RR | FDA UDI | Class II | Active |
| Endoplus | E337RR-45 | FDA UDI | Class II | Active |
| Endoplus | E338RR | FDA UDI | Class II | Active |
| Endoplus | E321MR-45 | FDA UDI | Class II | Active |
| Endoplus | 5553 | FDA UDI | Class II | Active |
| Endoplus | EN800L | FDA UDI | Class II | Active |
| Endoplus | E420RR-45 | FDA UDI | Class II | Active |
| Endoplus | 317VA | FDA UDI | Class II | Active |
| Endoplus | EN303 | FDA UDI | Class II | Active |
| Endoplus | 5326 | FDA UDI | Class II | Active |
| Endoplus | E340SLR | FDA UDI | Class II | Active |
| Endoplus | 5340L | FDA UDI | Class II | Active |
| Endoplus | E327SLR | FDA UDI | Class II | Active |
| Endoplus | E338R | FDA UDI | Class II | Active |
| Endoplus | E342M | FDA UDI | Class II | Active |
| Endoplus | 5374L | FDA UDI | Class II | Active |
| Endoplus | 5346L | FDA UDI | Class II | Active |
| Endoplus | E307DVR | FDA UDI | Class II | Active |
| Endoplus | 10RR | FDA UDI | Class II | Active |
| Endoplus | E363RR | FDA UDI | Class II | Active |
| Endoplus | E344MR | FDA UDI | Class II | Active |
| Endoplus | E323SLR-45 | FDA UDI | Class II | Active |
| Endoplus | su5652L | FDA UDI | Class II | Active |
| Endoplus | E342SR | FDA UDI | Class II | Active |
| Endoplus | E369DVR-45 | FDA UDI | Class II | Active |
| Endoplus | E302SL | FDA UDI | Class II | Active |
| Endoplus | E318MR | FDA UDI | Class II | Active |
| Endoplus | E336RR | FDA UDI | Class II | Active |
| Endoplus | E328RR | FDA UDI | Class II | Active |
| Endoplus | E333SLR-37 | FDA UDI | Class II | Active |
| Endoplus | EN301-45 | FDA UDI | Class II | Active |
| Endoplus | E336SLR-45 | FDA UDI | Class II | Active |
| Endoplus | EN320-45 | FDA UDI | Class II | Active |
| Endoplus | 5348L | FDA UDI | Class II | Active |
| Endoplus | E333SLR-32 | FDA UDI | Class II | Active |
| Endoplus | 5344L | FDA UDI | Class II | Active |
| Endoplus | E335SR-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. |