Contract manufacturerBeckman Coulter, Inc (Indianapolis, IN)IndianaClinical chemistryClass I
Beckman Coulter, Inc
Contract manufacturer ยท Indianapolis, IN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3007448124 (openFDA record; or search FDA's registration database)
- FEI number
- 3007448124
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- BECKMAN COULTER, INC. (FDA owner/operator no. 2050012)
- Registered address
- 5355 W. 76th Street, Indianapolis, IN 46268
- Contract listings
- 1 device listings, 1 product codes, first listed Jul 29, 2004
- 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 |
|---|---|---|---|---|---|
| JQC | Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use | Class I | Clinical chemistry | Contract manufacturing | Jul 29, 2004 |