Edge Systems Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Edge Systems Corp. makes
Edge Systems Corp. manufactures sterile tubing designed for medical and diagnostic applications, including fluid transfer and sample collection in clinical settings.
The company’s sterile tubing is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The product is based in the United States.
Catalogue
Del Sol Blue Light Therapy System Ref K061470
Regimes: 510(k) Registry: 510(k)Del Sol Red Light Therapy System Ref K072399
Regimes: 510(k) Registry: 510(k)Edge Systems Sterile Tubing Ref K990748
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Edge Systems Corp. have in the registry?
The registry currently lists 3 devices for Edge Systems Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Edge Systems Corp.'s devices?
Among its 3 most recently registered devices, Edge Systems Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Edge Systems Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Edge Systems Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Edge Systems Corp. in the registry?
The most recently registered devices listed for Edge Systems Corp. include DEL SOL BLUE LIGHT THERAPY SYSTEM, DEL SOL RED LIGHT THERAPY SYSTEM and EDGE SYSTEMS STERILE TUBING.