KLC SERVICES, INC./REEP

FDA Device Registration & Listing · London, OH, US · Registration 3007080244

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3007080244
FEI Number
3007080244
Entity Name
KLC SERVICES, INC./REEP
City/State/Country
London, OH, US
Establishment Address
215 US Highway 42 NE, London, OH 43140, US
Establishment Type(s)
Remanufacture Medical Device,Manufacture Medical Device
Owner / Operator
KLC Services, Inc./Reep (Owner Number: 10024510)
Owner / Operator Contact Address
215 US Highway 42 NE, London, OH 43140, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K950755
PMA Number
N/A

All Registered Proprietary Names

Flexmate S500 Flexmate K500

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BXB Exerciser, Powered Physical Medicine Class 1 890.5380 2008-02-07

Official Correspondent

Mark Reep

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KLC Services, Inc./Reep
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007080244. Last updated year: 2026. Please use registration number 3007080244 when referencing this establishment in official correspondence.
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