Data / Medical devices / Container, Specimen Mailer And Storage, Temperature Controlled, Sterile
Container, Specimen Mailer And Storage, Temperature Controlled, Sterile (KDW): 7 FDA-registered makers in 2 countries
7 establishments in 2 countries are registered with the FDA to make Container, Specimen Mailer And Storage, Temperature Controlled, Sterile (product code KDW, Class 1, 21 CFR 864.3250). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 4 510(k) clearances under this code, the latest on April 17, 1997, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- KDW
- Device class
- 1
- Regulation
- 864.3250
- Medical specialty
- Pathology
Makers by country
| Country | Makers |
|---|---|
| United States | 6 |
| China | 1 |
Makers of Container, Specimen Mailer And Storage, Temperature Controlled, Sterile
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 |
|---|---|---|---|---|---|---|---|---|
| Covidien | North Haven, CT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Covidien | Ponce, PR, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Paragon Medical - Mansfield, Bridgemedica | Mansfield, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STS Corporation | Duluth, GA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Venture Solutions | Arden Hills, MN, United States | Contract manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vericel Corporation | Cambridge, MA, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhejiang Mediunion Healthcare Group Co.,ltd | Ningbo Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated April 17, 1997. 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.