Silverleaf Medical Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Silverleaf Medical Products, Inc. makes
Silverleaf Medical Products, Inc. manufactures the PROSIT WOUND TREATMENT DEVICE and the CMB ANTIMICROBIAL DRESSING.
These devices are listed in the FDA 510(k) registry and are classified under device class U. The company is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Prosit Wound Treatment Device Ref K081977
Regimes: 510(k) Registry: 510(k)Cmb Antimicrobial Dressing Ref K060237
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Silverleaf Medical Products, Inc. have in the registry?
The registry currently lists 2 devices for Silverleaf Medical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Silverleaf Medical Products, Inc.'s devices?
Among its 2 most recently registered devices, Silverleaf Medical Products, Inc. has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Silverleaf Medical Products, Inc. in the registry?
The most recently registered devices listed for Silverleaf Medical Products, Inc. include PROSIT WOUND TREATMENT DEVICE and CMB ANTIMICROBIAL DRESSING.