Clearspec, LLC
Country not established
- Devices
- 16
What Clearspec, LLC makes
Clearspec, LLC manufactures single-use vaginal specula designed for clinical examinations. These disposable medical devices are intended for one-time use to facilitate gynecological procedures, ensuring hygiene and reducing cross-contamination risks.
The company’s products fall under Class II regulatory classification in the U.S., requiring premarket notification (510(k)) clearance through the FDA. The devices are listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations. The manufacturer operates from the United States.
Catalogue
Search and filter all 16 devicesCompany details
- DUNS number
- 075061406
Frequently asked questions
How many devices does Clearspec, LLC have in the registry?
The registry currently lists 16 devices for Clearspec, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clearspec, LLC's devices?
Among its 16 most recently registered devices, Clearspec, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (15 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Clearspec, LLC's devices fall under?
Among its 16 most recently registered devices, the classes recorded for Clearspec, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clearspec, LLC in the registry?
The most recently registered devices listed for Clearspec, LLC include ClearSpec 102, ClearSpec 103, ClearSpec 104 and ClearSpec 103NS.