Contract manufacturerOCCAM DESIGN (Louisville, KY)KentuckyGeneral and plastic surgeryNeurologyClass IClass II
OCCAM DESIGN
Contract manufacturer ยท Louisville, KY
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3008657524 (openFDA record; or search FDA's registration database)
- FEI number
- 3008657524
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Occam Design (FDA owner/operator no. 10033514)
- Registered address
- 1044 East Chestnuts St, Louisville, KY 40204
- Contract listings
- 3 device listings, 3 product codes, first listed Sep 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 |
|---|---|---|---|---|---|
| GBX | Catheter, Irrigation | Class I | General and plastic surgery | Contract manufacturing | Sep 16, 2022 |
| GWJ | Stimulator, Auditory, Evoked Response | Class II | Neurology | Contract manufacturing | May 27, 2026 |
| OMC | Reduced- Montage Standard Electroencephalograph | Class II | Neurology | Contract manufacturing | May 27, 2026 |