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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 14 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | 5RLS | FDA UDI | Class II | Active |
| Endoplus | 5RR | FDA UDI | Class II | Active |
| Endoplus | E323SLR | FDA UDI | Class II | Active |
| Endoplus | 5MRL | FDA UDI | Class II | Active |
| Endoplus | 364VL | FDA UDI | Class II | Active |
| Endoplus | E304MR | FDA UDI | Class II | Active |
| Endoplus | 341VL | FDA UDI | Class II | Active |
| Endoplus | 333VA | FDA UDI | Class II | Active |
| Endoplus | 5308 | FDA UDI | Class II | Active |
| Endoplus | E340RR | FDA UDI | Class II | Active |
| Endoplus | 5397 | FDA UDI | Class II | Active |
| Endoplus | E336RR-45 | FDA UDI | Class II | Active |
| Endoplus | E323SR | FDA UDI | Class II | Active |
| Endoplus | E302ACR | FDA UDI | Class II | Active |
| Endoplus | E333RR-45 | FDA UDI | Class II | Active |
| Endoplus | E320SR | FDA UDI | Class II | Active |
| Endoplus | E325ACR | FDA UDI | Class II | Active |
| Endoplus | 10434 | FDA UDI | Class II | Active |
| Endoplus | 5382L | FDA UDI | Class II | Active |
| Endoplus | E381SR | FDA UDI | Class II | Active |
| Endoplus | E382MR | FDA UDI | Class II | Active |
| Endoplus | E314RR | FDA UDI | Class II | Active |
| Endoplus | E414MR | FDA UDI | Class II | Active |
| Endoplus | E316M | FDA UDI | Class II | Active |
| Endoplus | 5349L | FDA UDI | Class II | Active |
| Endoplus | E307SR-45 | FDA UDI | Class II | Active |
| Endoplus | 5315L | FDA UDI | Class II | Active |
| Endoplus | 5321 | FDA UDI | Class II | Active |
| Endoplus | E420AC-45 | FDA UDI | Class II | Active |
| Endoplus | E377AC | FDA UDI | Class II | Active |
| Endoplus | E323S-37 | FDA UDI | Class II | Active |
| Endoplus | E324MR | FDA UDI | Class II | Active |
| Endoplus | E390DVR | FDA UDI | Class II | Active |
| Endoplus | 5RFRL | FDA UDI | Class II | Active |
| Endoplus | 10402L | FDA UDI | Class II | Active |
| Endoplus | E377RR-37 | FDA UDI | Class II | Active |
| Endoplus | E346RR-37 | FDA UDI | Class II | Active |
| Endoplus | EN803 | FDA UDI | Class II | Active |
| Endoplus | E314MR | FDA UDI | Class II | Active |
| Endoplus | 5364 | FDA UDI | Class II | Active |
| Endoplus | E309SLR | FDA UDI | Class II | Active |
| Endoplus | 5650J | FDA UDI | Class II | Active |
| Endoplus | 5345L | FDA UDI | Class II | Active |
| Endoplus | E339S | FDA UDI | Class II | Active |
| Endoplus | su5652J | FDA UDI | Class II | Active |
| Endoplus | E323S | FDA UDI | Class II | Active |
| Endoplus | E342MR-45 | FDA UDI | Class II | Active |
| Endoplus | 302VL | FDA UDI | Class II | Active |
| Endoplus | E327M-45 | FDA UDI | Class II | Active |
| Endoplus | E402SLR | 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. |