Silq Technologies, Corp.
United StatesFDA applicant, unverified
- Devices
- 7
What Silq Technologies, Corp. makes
Silq Technologies manufactures indwelling urethral drainage balloon catheters, including silicone-based models designed for urinary catheterization. The portfolio includes single-lumen and 2-way catheters intended for short- to intermediate-term bladder drainage.
These devices are classified as Class II under FDA regulations and are listed via 510(k) and UDI pathways. The company’s products are registered in the U.S. market.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
2-Way 100% Silicone ClearTract Catheter Ref K221625
Regimes: 510(k) Registry: 510(k)2-Way 100% Silicone Cleartract Catheter Ref K222118
Regimes: 510(k) Registry: 510(k)2-Way 100% Silicone Cleartract Catheter Ref K233013
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Silq Technologies, Corp. have in the registry?
The registry currently lists 7 devices for Silq Technologies, Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Silq Technologies, Corp.'s devices?
Among its 7 most recently registered devices, Silq Technologies, Corp. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Silq Technologies, Corp.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Silq Technologies, Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Silq Technologies, Corp. in the registry?
The most recently registered devices listed for Silq Technologies, Corp. include ClearTract 211410SPT, ClearTract 211605SPT, ClearTract 211810SPT and ClearTract 211610SPT.