Gtimd, LLC
United StatesFDA applicant, unverified
- Devices
- 3
What Gtimd, LLC makes
Gtimd, LLC manufactures cervical dilation devices, including the Aqueduct 100 Cervical Dilator and Aqueduct 100 Plus and 200 Cervical Dilation Balloon Catheters, designed for controlled cervical preparation in medical procedures.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Aqueduct 100 Cervical Dilator Ref K160664
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Aqueduct 200 Cervical Dilation Balloon Catheter Ref K202433
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gtimd, LLC have in the registry?
The registry currently lists 3 devices for Gtimd, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gtimd, LLC's devices?
Among its 3 most recently registered devices, Gtimd, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Gtimd, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Gtimd, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gtimd, LLC in the registry?
The most recently registered devices listed for Gtimd, LLC include Aqueduct 100 Cervical Dilator, Aqueduct 100 Plus Cervical Dilation Balloon Catheter and Aqueduct 200 Cervical Dilation Balloon Catheter.