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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 15 of 19| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Endoplus | 5303 | FDA UDI | Class II | Active |
| Endoplus | E377MR-37 | FDA UDI | Class II | Active |
| Endoplus | 5393L | FDA UDI | Class II | Active |
| Endoplus | E420RR-37 | FDA UDI | Class II | Active |
| Endoplus | 5362 | FDA UDI | Class II | Active |
| Endoplus | 5SLFRL | FDA UDI | Class II | Active |
| Endoplus | E393SLR | FDA UDI | Class II | Active |
| Endoplus | E375MR | FDA UDI | Class II | Active |
| Endoplus | E321AC-32 | FDA UDI | Class II | Active |
| Endoplus | 5MFRL | FDA UDI | Class II | Active |
| Endoplus | ES8500SLR | FDA UDI | Class II | Active |
| Endoplus | E334SR | FDA UDI | Class II | Active |
| Endoplus | E323RR-45 | FDA UDI | Class II | Active |
| Endoplus | E348SL | FDA UDI | Class II | Active |
| Endoplus | E377SLR-45 | FDA UDI | Class II | Active |
| Endoplus | E317SR | FDA UDI | Class II | Active |
| Endoplus | E323S-46 | FDA UDI | Class II | Active |
| Endoplus | E313S | FDA UDI | Class II | Active |
| Endoplus | E333SLR | FDA UDI | Class II | Active |
| Endoplus | E321SLR | FDA UDI | Class II | Active |
| Endoplus | 5313L | FDA UDI | Class II | Active |
| Endoplus | E339SLR | FDA UDI | Class II | Active |
| Endoplus | E393RR | FDA UDI | Class II | Active |
| Endoplus | E347RR | FDA UDI | Class II | Active |
| Endoplus | E361SR | FDA UDI | Class II | Active |
| Endoplus | E432SR | FDA UDI | Class II | Active |
| Endoplus | E327RR-45 | FDA UDI | Class II | Active |
| Endoplus | E346SL | FDA UDI | Class II | Active |
| Endoplus | 312VL | FDA UDI | Class II | Active |
| Endoplus | E324R | FDA UDI | Class II | Active |
| Endoplus | 5342L | FDA UDI | Class II | Active |
| Endoplus | E432RR | FDA UDI | Class II | Active |
| Richard Wolf | 8383.2937 | FDA UDI | Class II | Active |
| Endoplus | E304SR | FDA UDI | Class II | Active |
| Endoplus | E341MR | FDA UDI | Class II | Active |
| Endoplus | E333SR-37 | FDA UDI | Class II | Active |
| Endoplus | E321RR-45 | FDA UDI | Class II | Active |
| Endoplus | E328SR | FDA UDI | Class II | Active |
| Endoplus | E301MR | FDA UDI | Class II | Active |
| Endoplus | E317DVR-45 | FDA UDI | Class II | Active |
| Endoplus | 5333J | FDA UDI | Class II | Active |
| Endoplus | E333SL-45 | FDA UDI | Class II | Active |
| Endoplus | E321ACR | FDA UDI | Class II | Active |
| Endoplus | E329SR | FDA UDI | Class II | Active |
| Endoplus | EN301 | FDA UDI | Class II | Active |
| Richard Wolf | 8383.4897 | FDA UDI | Class II | Active |
| Endoplus | E312MR-45 | FDA UDI | Class II | Active |
| Endoplus | E369RR-45 | FDA UDI | Class II | Active |
| Endoplus | 5SLRNL | FDA UDI | Class II | Active |
| Endoplus | 5301L | 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. |