Contract manufacturerNeckCare Enterprises, Inc (Minneapolis, MN)MinnesotaOrthopedicPhysical medicineClass IClass II
NeckCare Enterprises, Inc
Contract manufacturer ยท Minneapolis, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3034089185 (openFDA record; or search FDA's registration database)
- FEI number
- 3034089185
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Contract manufacturer
- Owner or operator
- NeckCare Holding (FDA owner/operator no. 10084645)
- Registered address
- 520 Nicollet Mall Ste 710, Minneapolis, MN 55402
- Contract listings
- 2 device listings, 2 product codes, first listed Mar 16, 2022
- 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 |
|---|---|---|---|---|---|
| KQX | Goniometer, Ac-Powered | Class I | Orthopedic | Contract manufacturing | Mar 16, 2022 |
| QKC | Interactive Rehabilitation Exercise Device, Prescription Use | Class II | Physical medicine | Contract manufacturing | May 26, 2025 |