Contract manufacturerCadence Inc. (Staunton, VA)VirginiaGeneral and plastic surgeryOrthopedicNeurologyClass IClass II
Cadence Inc.
Contract manufacturer · Staunton, VA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3009266751 (openFDA record; or search FDA's registration database)
- FEI number
- 3009266751
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Cadence, Inc. (FDA owner/operator no. 2414164)
- Registered address
- 9 Technology Dr, Staunton, VA 24401
- Contract listings
- 4 device listings, 4 product codes, first listed Dec 13, 2012
- 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 |
|---|---|---|---|---|---|
| DWH | Blade, Saw, Surgical, Cardiovascular | Class I | General and plastic surgery | Contract manufacturing | Dec 17, 2012 |
| GFA | Blade, Saw, General & Plastic Surgery, Surgical | Class I | General and plastic surgery | Contract manufacturing | Dec 13, 2012 |
| LXH | Orthopedic Manual Surgical Instrument | Class I | Orthopedic | Contract manufacturing | Aug 11, 2023 |
| OLO | Orthopedic Stereotaxic Instrument | Class II | Neurology | Contract manufacturing | Sep 20, 2024 |