Lafayette Work Center, Inc

FDA Device Registration & Listing · Ballwin, MO, US · Registration 1931876

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
1931876
FEI Number
1000117913
Entity Name
Lafayette Work Center, Inc
City/State/Country
Ballwin, MO, US
Establishment Address
179 Gaywood Dr, Ballwin, MO 63021, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Lafayette Industries (Owner Number: 10046992)
Owner / Operator Contact Address
179 Gaywood Drive, Manchester, MO 63021, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Trademark catheter Childrens Splint

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KMK Device, Intravascular Catheter Securement General Hospital Class 1 880.5210 2014-06-10
NOC Splint, Extremity, Non-Inflatable, External, Non-Sterile General, Plastic Surgery Class 1 878.3910 2017-12-06
FYH Splint, Extremity, Noninflatable, External, Sterile General, Plastic Surgery Class 1 878.3910 2021-12-20

Official Correspondent

Robert Libera

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Lafayette Industries
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 1931876. Last updated year: 2026. Please use registration number 1931876 when referencing this establishment in official correspondence.
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