Data / Medical devices / United States / Radcliffe Watts, LLC
Radcliffe Watts, LLC: FDA-registered device maker in Mansfield, OH, United States, 1 510(k) clearance
Radcliffe Watts, LLC is registered with the FDA (registration 3045522560) in Mansfield, OH, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 4, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3045522560
- Address
- 201 E 5th St, Mansfield, OH, United States, 44902
- Owner or operator
- Radcliffe Watts, LLC (10095964)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- May 31, 2026
- Registered through
- 2026
- Brand names listed
- Klar Lite, RCW-KL1000
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light, Ultraviolet, Dermatological | FTC | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 4, 2026 | K253871 | Klär Lite (RCW-KL1000) | FTC | Substantially Equivalent | Radcliffe Watts, LLC | accessdata.fda.gov |
Compare with other makers
Updated March 4, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.