Ingfertility, LLC
Country not established
- Devices
- 1
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Pre-Va Vaginal Lubricant Ref K072741
Regimes: 510(k) Registry: 510(k)
FDA recalls
2008
- 22 Sep 2008 Z-0626-2009 Unclassified (pre-2012) Terminated Product contaminated with bacteria (Brachybacterium rhamnosum, a non pathogen gram positive cocci).
Frequently asked questions
How many devices does Ingfertility, LLC have in the registry?
The registry currently lists 1 device for Ingfertility, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ingfertility, LLC's devices?
Among its 1 most recently registered device, Ingfertility, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Ingfertility, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ingfertility, LLC's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Ingfertility, LLC?
FDA recall records list 1 recall initiated by Ingfertility, LLC, the most recent initiated on 22 Sep 2008. 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 Ingfertility, LLC in the registry?
The most recently registered devices listed for Ingfertility, LLC include PRE-VA VAGINAL LUBRICANT.