I.L. Med, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What I.L. Med, Inc. makes
I.L. Med, Inc. manufactures the CODMAN NEUROLASE LASER SYSTEM, a medical device designed for neurosurgical applications, including modifications of the original system. This laser system is intended for precise tissue ablation and coagulation in spinal and cranial procedures.
The company’s portfolio is regulated under FDA Class II devices, with authorisation supported by 510(k) clearances. The devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Codman Neurolase Laser System Ref K883642
510(k) 510(k)Codman Neurolase Laser System/Modification Ref K905511
510(k) 510(k)
Frequently asked questions
How many devices does I.L. Med, Inc. have in the registry?
The registry currently lists 2 devices for I.L. Med, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list I.L. Med, Inc.'s devices?
Among its 2 most recently registered devices, I.L. Med, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do I.L. Med, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for I.L. Med, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from I.L. Med, Inc. in the registry?
The most recently registered devices listed for I.L. Med, Inc. include CODMAN NEUROLASE LASER SYSTEM and CODMAN NEUROLASE LASER SYSTEM/MODIFICATION.