Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004571972

FEI Number

3004571972

Entity Name

AMA OPTICS, INC.

City/State/Country

Miami Beach, FL, US

Establishment Address

1410 Sunset Harbour Dr Ste 208, Miami Beach, FL 33139, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

AMA OPTICS, INC. (Owner Number: 9063607)

Owner / Operator Contact Address

1410 Sunset Harbour Drive, Suite 208, Miami Beach, FL 33139, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Panoramic Pinhole Lens AMA Optics Vision Aid RAM Near Lens Pinhole Clip DiagnosticGame AMA Optics Occluder NeuroColor AMA Optics Frames AMA Optics Calibrator Retinal Acuity Meter (RAM) Brightness Acuity Meter (BAM) RAM ETDRS RAM Solo Modular RAM PRIME XL RAM PRIME RAM Solo

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HPC	Set, Lens, Trial, Ophthalmic	Ophthalmic	Class 1	886.1405	2008-12-07
HPE	Aid, Vision, Optical, Battery-Powered	Ophthalmic	Class 1	886.5915	2023-07-26
HPB	Clip, Lens, Trial, Ophthalmic	Ophthalmic	Class 1	886.1410	2008-12-07
HLC	Instrument, Measuring, Stereopsis	Ophthalmic	Class 1	886.1460	2014-05-21
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2023-07-26
HIT	Tester, Color Vision	Ophthalmic	Class 1	886.1170	2014-05-21
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2023-07-19
FTY	Tape, Measuring, Rulers And Calipers	General, Plastic Surgery	Class 1	878.4800	2023-07-25
HOX	Chart, Visual Acuity	Ophthalmic	Class 1	886.1150	2004-05-19

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AMA OPTICS, 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
K900478	Woodlyn, Inc.	WOODLYN FULL APERTURE TRIAL LENS SET	1990-02-21
K910951	United Optical, Spa	OPTHLAMIC FRAMES	1991-05-06

Similar Registrations

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3003039352	EPSILON EYE CARE PVT., LTD.	MUMBAI Maharashtra, IN
8040382	PAUL INSTRUMENTS (INDIA)	CALCUTTA West Bengal, IN
3042228518	AKRITI OPHTHALMIC PRIVATE LIMITED	Hyderabad Telangana, IN
3003951061	M/S TARUN ENTERPRISES	Prayagraj, Uttar Pradesh, IN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004571972. Last updated year: 2026. Please use registration number 3004571972 when referencing this establishment in official correspondence.