Idev Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 11
- FDA recalls
- 2
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Search and filter all 11 devicesFDA recalls
2012
- 29 May 2012 Z-1550-2013 Class II Terminated There was an error on the outer labeling of this device. The inner label was correct.
- 31 Jan 2012 Z-1213-2012 Not yet classified Terminated The firm is taking this action because the device was one of eight that may have been mislabeled with the incorrect size (length).
Frequently asked questions
How many devices does Idev Technologies, Inc. have in the registry?
The registry currently lists 11 devices for Idev Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Idev Technologies, Inc.'s devices?
Among its 11 most recently registered devices, Idev Technologies, Inc. has devices listed in FDA 510(k) (11 devices).
What risk classes do Idev Technologies, Inc.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Idev Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Idev Technologies, Inc.?
FDA recall records list 2 recalls initiated by Idev Technologies, Inc., the most recent initiated on 29 May 2012. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Idev Technologies, Inc. in the registry?
The most recently registered devices listed for Idev Technologies, Inc. include SUPERA VERITAS(R) INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM, SUPERA INTERWOVEN SELF-EXPANDING BILIARY NITINOL STENT DELIVERY CATHETER, MODEL # S-04-040-120, AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL 10060060 and SUPERA VERITAS INTERWOVEN SELF-EXPANDING NITINOL STENT TRANSHEPATIC BILIARY SYSTEM.