NICEFY INC

FDA Device Registration & Listing · Torrance, CA, US · Registration 3030434441

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
3030434441
FEI Number
3030434441
Entity Name
NICEFY INC
City/State/Country
Torrance, CA, US
Establishment Address
3135 Kashiwa St, STE B, Torrance, CA 90505, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
NICEFY INC (Owner Number: 10089668)
Owner / Operator Contact Address
3135 Kashiwa St, STE B, Torrance, CA 90505, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

GRINDERPUNCH

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NJH Lens, Spectacle (Prescription), For Reading Discomfort Ophthalmic Class 1 886.5844 2023-12-27

Official Correspondent

Tancredi Ingrassia

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NICEFY INC
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 3030434441. Last updated year: 2026. Please use registration number 3030434441 when referencing this establishment in official correspondence.
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