Het Systems, LLC
United StatesFDA applicant, unverified
- Devices
- 3
What Het Systems, LLC makes
Het Systems, LLC manufactures bipolar electrocautery forceps and bipolar ligator systems designed for surgical tissue sealing and cutting. These devices are intended for use in minimally invasive procedures to reduce bleeding and improve precision during operations.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. Het Systems, LLC is based in the United States.
Catalogue
Het Bipolar Electrocautery Forceps Ref K110143
Regimes: 510(k) Registry: 510(k)Het Bipolar Ligator System Ref K121085
Regimes: 510(k) Registry: 510(k)Het Systems, LLC, Het Bipolar Ligator System Ref K140422
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Het Systems, LLC have in the registry?
The registry currently lists 3 devices for Het Systems, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Het Systems, LLC's devices?
Among its 3 most recently registered devices, Het Systems, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Het Systems, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Het Systems, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Het Systems, LLC in the registry?
The most recently registered devices listed for Het Systems, LLC include HET BIPOLAR ELECTROCAUTERY FORCEPS, HET BIPOLAR LIGATOR SYSTEM and HET SYSTEMS, LLC, HET BIPOLAR LIGATOR SYSTEM.