Neometrics, Inc.
United StatesFDA applicant, unverified
- Devices
- 21
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Search and filter all 21 devicesFDA recalls
2014
- 31 Mar 2014 Z-1747-2014 Class II Terminated Neo Metrics, Inc. is recalling NovaGold Guidewire because the tip may uncoil and / detach more frequently than anticipated. There have been no reports of illness or injury.
Full distribution text
- 31 Mar 2014 Z-1747-2014 Class II Terminated Neo Metrics, Inc. is recalling NovaGold Guidewire because the tip may uncoil and / detach more frequently than anticipated. There have been no reports of illness or injury.
Frequently asked questions
How many devices does Neometrics, Inc. have in the registry?
The registry currently lists 21 devices for Neometrics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neometrics, Inc.'s devices?
Among its 21 most recently registered devices, Neometrics, Inc. has devices listed in FDA 510(k) (21 devices).
What risk classes do Neometrics, Inc.'s devices fall under?
Among its 21 most recently registered devices, the classes recorded for Neometrics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Neometrics, Inc.?
FDA recall records list 1 recall initiated by Neometrics, Inc., the most recent initiated on 31 Mar 2014. 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 Neometrics, Inc. in the registry?
The most recently registered devices listed for Neometrics, Inc. include ACCUSCREEN T4, VASCUPUNCTURE PICC GUIDEWIRE WITH HYDRO-SILK COATING, SELECTIVA GUIDEWIRE and VASCUPUNCTURE PICC GUIDEWIRE.