This page includes the latest FDA filings for Serendia L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3014498773 |
| FEI Number | 3014498773 |
| Name | SERENDIA LLC |
| Owner & Operator | Serendia LLC |
| Contact Address | 23865 Via Del Rio Yorba Linda CA 92887 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | Y |
| Registration Expiration | 2020-04-25 |
| Registration Address | 23865 Via Del Rio Yorba Linda, CA 92887 US |
| Establishment Type | Develop Specifications But Do Not Manufacture At This Facility |
Device Company | Device | Date |
|---|---|---|
SERENDIA LLC | CELFIRM | 2018-05-22 |
| Import ID | Shipment | Cargo Description | Quantity |
|---|---|---|---|
| 2020053042704 | Pusan,South Korea -> Long Beach, California | OTHER MEDICAL INSTRUMENT 9018.90-9080 | 7 PKG |
| 2020042763882 | Pusan,South Korea -> Los Angeles, California | SCARLET SRF (MEDICAL DEVICE) | 30 PKG |
| 2018100322358 | Pusan,South Korea -> New York/Newark Area, Newark, New Jersey | MEDICAL INSTRUMENT | 1 PKG |
| 2018091754564 | Pusan,South Korea -> Los Angeles, California | MEDICAL INSTRUMENT | 3 PKG |
| 2018091754565 | Pusan,South Korea -> Los Angeles, California | MEDICAL INSTRUMENT | 1 PKG |
| 2018080364856 | Pusan,South Korea -> Los Angeles, California | SCARLET S | 12 PKG |