CRYSTAL OPTICS MANUFACTURE LTD

FDA Device Registration & Listing · Acco Haifa, IL · Registration 3008939601

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
3008939601
FEI Number
3008939601
Entity Name
CRYSTAL OPTICS MANUFACTURE LTD
City/State/Country
Acco Haifa, IL
Establishment Address
Moshe Burrenstien 11, Acco Haifa 2422233, IL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Crystal Optics Manufacture Ltd (Owner Number: 10051664)
Owner / Operator Contact Address
Moshe Burrenstien 11, Acco, IL-HA 2422233, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Lens, Spectacle, Non-Custom (Prescription) Lens, Spectacle (Prescription), For Reading Discomfort

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2016-04-18
NJH Lens, Spectacle (Prescription), For Reading Discomfort Ophthalmic Class 1 886.5844 2016-04-18

Official Correspondent

No official correspondent registered.

US Agent Details

jay Mansour Business: Mansour Consulting LLC Email: jay@mansourconsulting.com Phone: (678) 6789088

Related Public Records

Same Entity

Crystal Optics Manufacture Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008939601. Last updated year: 2026. Please use registration number 3008939601 when referencing this establishment in official correspondence.
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