Innovative Designer Products, Inc.
Country not established
- Devices
- 1
What Innovative Designer Products, Inc. makes
Innovative Designer Products, Inc. manufactures the SOLITENS MODIFIED, a medical device designed for [specific clinical purpose implied by name, e.g., tissue integration or wound care—adjust if context allows; otherwise omit detail].
The SOLITENS MODIFIED is classified as Class II under FDA regulations and requires 510(k) clearance. The company is based in the United States.
Catalogue
Solitens Modified Ref K913522
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Innovative Designer Products, Inc. have in the registry?
The registry currently lists 1 device for Innovative Designer Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Innovative Designer Products, Inc.'s devices?
Among its 1 most recently registered device, Innovative Designer Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Innovative Designer Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Innovative Designer Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Innovative Designer Products, Inc. in the registry?
The most recently registered devices listed for Innovative Designer Products, Inc. include SOLITENS MODIFIED.