Lange Medical Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Multidex Hydrophilic Wound Dressing Ref K945000
Regimes: 510(k) Registry: 510(k)Multidex Hydrophilic Wound Dressing Gel Ref K962917
Regimes: 510(k) Registry: 510(k)Multidex Plus Hydrophilic Wound Dressing Ref K955399
Regimes: 510(k) Registry: 510(k)Multidex Gel Ref K952774
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lange Medical Products, Inc. have in the registry?
The registry currently lists 4 devices for Lange Medical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lange Medical Products, Inc.'s devices?
Among its 4 most recently registered devices, Lange Medical Products, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Lange Medical Products, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Lange Medical Products, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Lange Medical Products, Inc. in the registry?
The most recently registered devices listed for Lange Medical Products, Inc. include MULTIDEX HYDROPHILIC WOUND DRESSING, MULTIDEX HYDROPHILIC WOUND DRESSING GEL, MULTIDEX PLUS HYDROPHILIC WOUND DRESSING and MULTIDEX GEL.