Contract manufacturerComar (Rancho Cucamonga, CA)CaliforniaHematologyClass II
Comar
Contract manufacturer ยท Rancho Cucamonga, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3004601221 (openFDA record; or search FDA's registration database)
- FEI number
- 3004601221
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Comar LLC / PCI (FDA owner/operator no. 9084326)
- Registered address
- 9595 Utica Ave, Rancho Cucamonga, CA 91730
- Contract listings
- 1 device listings, 1 product codes, first listed Sep 2, 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 |
|---|---|---|---|---|---|
| GKT | Separator, Automated, Blood Cell, Diagnostic | Class II | Hematology | Contract manufacturing | Sep 2, 2022 |