MINUS PLUS LLC

FDA Device Registration & Listing · Los Angeles, CA, US · Registration 3014539734

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
3014539734
FEI Number
3014539734
Entity Name
MINUS PLUS LLC
City/State/Country
Los Angeles, CA, US
Establishment Address
2801 N San Fernando Rd, Unit C, Los Angeles, CA 90065, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Minus Plus LLC (Owner Number: 10058014)
Owner / Operator Contact Address
2801 N San Fernando Rd, Unit C, Los Angeles, CA 90065, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AKILA Akila

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOI Spectacle, Magnifying Ophthalmic Class 1 886.5840 2018-06-26
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2020-01-16

Official Correspondent

Steven Bates

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Minus Plus LLC
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
K910951 United Optical, Spa OPTHLAMIC FRAMES 1991-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014539734. Last updated year: 2026. Please use registration number 3014539734 when referencing this establishment in official correspondence.
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