Syntech Development Manufacturing

FDA Filings

This page includes the latest FDA filings for Syntech Development Manufacturing. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3008280537
FEI Number3008280537
NameSyntech Development & Manufacturing
Owner & OperatorSyntech Development & Manufacturing/Nelson
Contact Address13948 Mountain Ave
Chino CA 91710 US
Official Correspondent
  • Staci Nelson
  • x-909-4655554-14
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address13948 Mountain Ave
Chino, CA 91710 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Syntech Development & Manufacturing [Syntech Development & Manufacturing/Nelson]
Set, i.V. Fluid transfer2013-01-21
Syntech Development & Manufacturing [Syntech Development & Manufacturing/Nelson]
System, peritoneal, automatic delivery2013-01-21
Syntech Development & Manufacturing [Syntech Development & Manufacturing/Nelson]
Set, administration, intravascular2013-01-21

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