Contract manufacturerD&K Engineering (San Diego, CA)CaliforniaClinical chemistryNeurologyClass IClass II
D&K Engineering
Contract manufacturer ยท San Diego, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3005268307 (openFDA record; or search FDA's registration database)
- FEI number
- 3005268307
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- D&K Engineering (FDA owner/operator no. 10044530)
- Registered address
- 15890 Bernardo Center Dr, San Diego, CA 92127
- Contract listings
- 2 device listings, 3 product codes, first listed Jun 24, 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 |
|---|---|---|---|---|---|
| JQW | Station, Pipetting And Diluting, For Clinical Use | Class I | Clinical chemistry | Contract manufacturing | Jun 24, 2013 |
| OBP | Transcranial Magnetic Stimulator | Class II | Neurology | Contract manufacturing | Apr 9, 2025 |
| QCI | Transcranial Magnetic Stimulation System For Obsessive-Compulsive Disorder | Class II | Neurology | Contract manufacturing | Apr 9, 2025 |