Data / Medical devices / United States / KLC Services, Inc./Reep
KLC Services, Inc./Reep: FDA-registered device maker in London, OH, United States, 1 510(k) clearance
KLC Services, Inc./Reep is registered with the FDA (registration 3007080244) in London, OH, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 5, 1995. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007080244
- Address
- 215 US Highway 42 NE, London, OH, United States, 43140
- Owner or operator
- KLC Services, Inc./Reep (10024510)
- Roles
- Manufacturer, Remanufacturer
- First device listed
- February 7, 2008
- Registered through
- 2026
- Brand names listed
- Flexmate K500, Flexmate S500
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Exerciser, Powered | BXB | 1 | Manufacturer, Remanufacturer | 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 |
|---|---|---|---|---|---|---|
| October 5, 1995 | K950755 | FLEXMATE K500 | BXB | Substantially Equivalent | Breg, Inc. | accessdata.fda.gov |
Compare with other makers
Updated October 5, 1995. 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.