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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 11 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | E347SR-45 | FDA UDI | Class II | Active |
| Endoplus | 5297 | FDA UDI | Class II | Active |
| Endoplus | E434S | FDA UDI | Class II | Active |
| Endoplus | E378MR-45 | FDA UDI | Class II | Active |
| Endoplus | 10420 | FDA UDI | Class II | Active |
| Endoplus | 5376L | FDA UDI | Class II | Active |
| Endoplus | EN804 | FDA UDI | Class II | Active |
| Endoplus | 5XFRL | FDA UDI | Class II | Unknown |
| Endoplus | E334RR | FDA UDI | Class II | Active |
| Endoplus | E340ACR | FDA UDI | Class II | Active |
| Endoplus | 10414 | FDA UDI | Class II | Active |
| Endoplus | 5333 | FDA UDI | Class II | Active |
| Endoplus | su5651 | FDA UDI | Class II | Active |
| Endoplus | EN805L | FDA UDI | Class II | Active |
| Endoplus | E335MR | FDA UDI | Class II | Active |
| Endoplus | 5361L | FDA UDI | Class II | Active |
| Endoplus | E338DVR | FDA UDI | Class II | Active |
| Endoplus | 5150 | FDA UDI | Class II | Active |
| Endoplus | E309M | FDA UDI | Class II | Active |
| Endoplus | 304VL | FDA UDI | Class II | Active |
| Endoplus | 5324L | FDA UDI | Class II | Active |
| Endoplus | 5336L | FDA UDI | Class II | Active |
| Endoplus | su5650 | FDA UDI | Class II | Active |
| Endoplus | 5347 | FDA UDI | Class II | Active |
| Endoplus | EN702L | FDA UDI | Class II | Active |
| Endoplus | E333MR-37 | FDA UDI | Class II | Active |
| Endoplus | E319MR | FDA UDI | Class II | Active |
| Endoplus | 5313 | FDA UDI | Class II | Active |
| Endoplus | E361RR | FDA UDI | Class II | Active |
| Endoplus | 5380L | FDA UDI | Class II | Active |
| Endoplus | 5302 | FDA UDI | Class II | Active |
| Richard Wolf | 8383.4895 | FDA UDI | Class II | Active |
| Endoplus | E332RR | FDA UDI | Class II | Active |
| Endoplus | E302SLR | FDA UDI | Class II | Active |
| Endoplus | E362MR | FDA UDI | Class II | Active |
| Endoplus | E312M | FDA UDI | Class II | Active |
| Endoplus | E412S | FDA UDI | Class II | Active |
| Endoplus | E317RR | FDA UDI | Class II | Active |
| Endoplus | E394MR | FDA UDI | Class II | Active |
| Endoplus | E325M | FDA UDI | Class II | Active |
| Endoplus | E315MR | FDA UDI | Class II | Active |
| Endoplus | 5394L | FDA UDI | Class II | Active |
| Endoplus | EN315 | FDA UDI | Class II | Active |
| Endoplus | E328AC-45 | FDA UDI | Class II | Active |
| Endoplus | E331M-25 | FDA UDI | Class II | Active |
| Endoplus | 5390 | FDA UDI | Class II | Active |
| Richard Wolf | 8383.2927 | FDA UDI | Class II | Active |
| Endoplus | E424AC | FDA UDI | Class II | Active |
| Endoplus | su5850 | FDA UDI | Class II | Active |
| Endoplus | E432SLR-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. |