Data / Medical devices / Cord Blood Processing System And Storage Container
Cord Blood Processing System And Storage Container (OAO): 7 FDA-registered makers in 4 countries
7 establishments in 4 countries are registered with the FDA to make Cord Blood Processing System And Storage Container (product code OAO, Class 2, 21 CFR 864.9900). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- OAO
- Device class
- 2
- Regulation
- 864.9900
- Medical specialty
- Hematology
Makers by country
| Country | Makers |
|---|---|
| United States | 3 |
| Mexico | 2 |
| United Kingdom | 1 |
| Switzerland | 1 |
Makers of Cord Blood Processing System And Storage Container
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Avances Cientificos de Mexico | H. Matamoros Tamaulipas, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Centerpiece S. De R.L De C.V | Playas de Rosarito Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cryo-Cell International, Inc. | Oldsmar, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Global Life Sciences Solutions USA LLC | Marlborough, MA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pall Newquay | Newquay Cornwall, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pall International, Sarl | Fribourg, Switzerland | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ThermoGenesis Corp. | Rancho Cordova, CA, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.