BLAINE LABS, INC.

FDA Device Registration & Listing · SANTA FE SPRINGS, CA, US · Registration 3001744192

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
3001744192
FEI Number
3001744192
Entity Name
BLAINE LABS, INC.
City/State/Country
SANTA FE SPRINGS, CA, US
Establishment Address
11037 LOCKPORT PLACE, SANTA FE SPRINGS, CA 90670, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
BLAINE LABS, INC. (Owner Number: 9043971)
Owner / Operator Contact Address
11037 LOCKPORT PLACE, --, Santa Fe Springs, CA 90670, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Vibration Anesthesia Device

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IRO Vibrator, Therapeutic Physical Medicine Class 1 890.5975 2010-09-03

Official Correspondent

ROBERT BLAINE

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BLAINE LABS, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K821133 Durham Electric Co. ELECTRICAL VIBRATING DEVICE 1982-07-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001744192. Last updated year: 2026. Please use registration number 3001744192 when referencing this establishment in official correspondence.
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