Hmt, Inc.
South KoreaFDA applicant, unverified
- Devices
- 1
What Hmt, Inc. makes
Hmt, Inc. manufactures the HMT 21 and HMT 2000 Urinary Incontinence System, which are medical devices designed to treat urinary incontinence.
These devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Hmt 21, Hmt 2000 Urinary Incontinence System Ref K011435
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hmt, Inc. have in the registry?
The registry currently lists 1 device for Hmt, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hmt, Inc.'s devices?
Among its 1 most recently registered device, Hmt, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hmt, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hmt, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hmt, Inc. in the registry?
The most recently registered devices listed for Hmt, Inc. include HMT 21, HMT 2000 URINARY INCONTINENCE SYSTEM.