LINDAR CORPORATION

FDA Device Registration & Listing · Baxter, MN, US · Registration 3008431074

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
3008431074
FEI Number
3008431074
Entity Name
LINDAR CORPORATION
City/State/Country
Baxter, MN, US
Establishment Address
7789 Hastings Road, Baxter, MN 56425, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
LINDAR Corporation (Owner Number: 10090788)
Owner / Operator Contact Address
7789 Hastings Road, Baxter, MN 56425, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

zPods

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OYS Patient Bed With Canopy/Restraints General Hospital Class 1 880.6760 2024-05-14

Official Correspondent

Mary Richards

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LINDAR Corporation
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 3008431074. Last updated year: 2026. Please use registration number 3008431074 when referencing this establishment in official correspondence.
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