Milex Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 8
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Curette, Proposed Tis-U-Trap, Metal Ref K760264
Regimes: 510(k) Registry: 510(k)Inflat-O-Ball Ref K904026
Regimes: 510(k) Registry: 510(k)Milex Kegel Perineal Exerciser Ref K862410
Regimes: 510(k) Registry: 510(k)Kopans Hookwire Lesion Localization Needle Ref K900903
Regimes: 510(k) Registry: 510(k)Pipet Curet Ref K001545
Regimes: 510(k) Registry: 510(k)Inglat-O-Ball Ref K904774
Regimes: 510(k) Registry: 510(k)Endo C Brush Ref K882628
Regimes: 510(k) Registry: 510(k)Milex Bartholin Gland Catheter Ref K861385
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Milex Products, Inc. have in the registry?
The registry currently lists 8 devices for Milex Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Milex Products, Inc.'s devices?
Among its 8 most recently registered devices, Milex Products, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Milex Products, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Milex Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Milex Products, Inc. in the registry?
The most recently registered devices listed for Milex Products, Inc. include CURETTE, PROPOSED TIS-U-TRAP, METAL, INFLAT-O-BALL, MILEX KEGEL PERINEAL EXERCISER and KOPANS HOOKWIRE LESION LOCALIZATION NEEDLE.