Contract manufacturerCirtec Medical (Santa Clara, CA)CaliforniaCardiovascularClass II
Cirtec Medical
Contract manufacturer · Santa Clara, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3004737415 (openFDA record; or search FDA's registration database)
- FEI number
- 3004737415
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Cirtec Medical Corporation (FDA owner/operator no. 10025422)
- Registered address
- 3301 Leonard Ct., Santa Clara, CA 95054
- Contract listings
- 4 device listings, 3 product codes, first listed May 10, 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 |
|---|---|---|---|---|---|
| DQO | Catheter, Intravascular, Diagnostic | Class II | Cardiovascular | Contract manufacturing | Apr 17, 2024 |
| DYB | Introducer, Catheter | Class II | Cardiovascular | Contract manufacturing | Oct 31, 2024 |
| QEW | Peripheral Mechanical Thrombectomy With Aspiration | Class II | Cardiovascular | Contract manufacturing | May 10, 2022 |