Contract manufacturerENDOPLUS (Mundelein, IL)IllinoisGeneral and plastic surgeryNeurologyClass II
ENDOPLUS
Contract manufacturer · Mundelein, IL
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 1423714 (openFDA record; or search FDA's registration database)
- FEI number
- 3000719482
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- ENDOPLUS (FDA owner/operator no. 9005786)
- Registered address
- 750 Tower Rd Ste A, Mundelein, IL 60060
- Contract listings
- 2 device listings, 2 product codes, first listed Jan 30, 2013
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | Class II | General and plastic surgery | Contract manufacturing | Feb 24, 2026 |
| HBG | Drills, Burrs, Trephines & Accessories (Manual) | Class II | Neurology | Contract manufacturing | Jan 30, 2013 |