THE SIDE LYER COMPANY

FDA Device Registration & Listing · Orlando, FL, US · Registration 3030492371

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
3030492371
FEI Number
3030492371
Entity Name
THE SIDE LYER COMPANY
City/State/Country
Orlando, FL, US
Establishment Address
1509 E. Colonial Drive, Ste. 300, Orlando, FL 32803, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
The Side Lyer Company (Owner Number: 10090060)
Owner / Operator Contact Address
1509 E. Colonial Drive, Ste. 300, Orlando, FL 32803, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Side Lyer SideLyer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKZ Bed, Patient Rotation, Powered Physical Medicine Class 2 890.5225 2024-02-08

Official Correspondent

Erica Plazibat

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Side Lyer Company
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030492371. Last updated year: 2026. Please use registration number 3030492371 when referencing this establishment in official correspondence.
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