I For M, Inc.
Country not established
- Devices
- 1
What I For M, Inc. makes
I For M, Inc. manufactures the I-GLIDE IOL Implantation Aid, a device designed to assist in the insertion of intraocular lenses (IOLs) during cataract surgery.
The I-GLIDE IOL Implantation Aid is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
I-Glide IOL Implantation Aid Ref K832939
510(k) 510(k)
Frequently asked questions
How many devices does I For M, Inc. have in the registry?
The registry currently lists 1 device for I For M, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list I For M, Inc.'s devices?
Among its 1 most recently registered device, I For M, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do I For M, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for I For M, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from I For M, Inc. in the registry?
The most recently registered devices listed for I For M, Inc. include I-GLIDE IOL IMPLANTATION AID.