This page includes the latest FDA filings for Vericel. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 1226230 |
| FEI Number | 3002836339 |
| Name | Vericel Corporation |
| Owner & Operator | Vericel |
| Contact Address | 64 Sydney Street Cambridge MA 02139 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 64 Sidney St CAMBRIDGE, MA 02139 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
Vericel Corporation [Vericel] | cultured epithelial autograft | 2016-02-04 |
Vericel Corporation [Vericel] | container, specimen mailer and storage, temperature controlled, sterile | 2016-02-04 |
Vericel Corporation [Vericel] | kit, surgical instrument, disposable | 2016-02-04 |