This page includes the latest FDA filings for Syntech Development Manufacturing Nelson. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3000299546 |
FEI Number | 3000299546 |
Name | ACCENT PLASTICS |
Owner & Operator | Syntech Development & Manufacturing/Nelson |
Contact Address | 13948 Mountain Ave Chino CA 91710 US |
Official Correspondent |
|
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 1925 ELISE CIRCLE CORONA, CA 92879 US |
Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Registration Number | 3008280537 |
FEI Number | 3008280537 |
Name | Syntech Development & Manufacturing |
Owner & Operator | Syntech Development & Manufacturing/Nelson |
Contact Address | 13948 Mountain Ave Chino CA 91710 US |
Official Correspondent |
|
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 13948 Mountain Ave Chino, CA 91710 US |
Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
---|---|---|
ACCENT PLASTICS [Syntech Development & Manufacturing/Nelson] | Klenzalac; Splashield; Supershield; Zerowet | 2020-01-24 |
Syntech Development & Manufacturing [Syntech Development & Manufacturing/Nelson] | Set, i.V. Fluid transfer | 2013-01-21 |
Syntech Development & Manufacturing [Syntech Development & Manufacturing/Nelson] | System, peritoneal, automatic delivery | 2013-01-21 |
Syntech Development & Manufacturing [Syntech Development & Manufacturing/Nelson] | Set, administration, intravascular | 2013-01-21 |