Contract manufacturerMEDBIO, LLC. (Grand Rapids, MI)MichiganCardiovascularGastroenterology and urologyClinical chemistryClass IIClass IClass III
MEDBIO, LLC.
Contract manufacturer · Grand Rapids, MI
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3009810261 (openFDA record; or search FDA's registration database)
- FEI number
- 3009810261
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer; Repackager or relabeler
- Owner or operator
- Medbio, LLC (FDA owner/operator no. 10044061)
- Registered address
- 5346 36th St SE, Grand Rapids, MI 49512
- Contract listings
- 4 device listings, 4 product codes, first listed Aug 11, 2014
- 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 |
|---|---|---|---|---|---|
| DXC | Clamp, Vascular | Class II | Cardiovascular | Contract manufacturing | Aug 11, 2014 |
| NOA | Device, Paste-On For Incontinence, Non-Sterile | Class I | Gastroenterology and urology | Contract manufacturing | Feb 19, 2025 |
| QCD | Continuous Glucose Monitor, Implanted, Adjunctive Use | Class III | Clinical chemistry | Contract manufacturing | Nov 18, 2019 |
| QHJ | Sensor, Glucose, Implanted, Non-Adjunctive Use | Class III | Clinical chemistry | Contract manufacturing | Nov 18, 2019 |