Skip to content

Syntech, Int'l Inc.

United Statesfrom the FDA registration address FDA establishment FEI 3005142514

Devices
11
Registrations
FDA
FDA recalls
0

Catalogue11

Newest first, rows 1-11 of 11

Search and filter all 11 devices
Skip device list

Rows 1-11 of 11

Company details

FDA FEI number
3005142514
Address
17171 DAIMLER AVE., IRVINE, CA, 92614

Frequently asked questions

How many devices does SYNTECH, INT'L INC. have in the registry?

The registry currently lists 11 devices for SYNTECH, INT'L INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list SYNTECH, INT'L INC.'s devices?

Among its 11 most recently registered devices, SYNTECH, INT'L INC. has devices listed in FDA GUDID (11 devices).

What risk classes do SYNTECH, INT'L INC.'s devices fall under?

Among its 11 most recently registered devices, the classes recorded for SYNTECH, INT'L INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from SYNTECH, INT'L INC. in the registry?

The most recently registered devices listed for SYNTECH, INT'L INC. include MAXAIR 2281PRS-100, MAXAIR 2084-04-PR, MAXAIR 2500-37TSC-PR and MAXAIR 2500-36TSC-PR.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.