NICTAVI

FDA Device Registration & Listing · Los Angeles, CA, US · Registration 3017733452

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
3017733452
FEI Number
3017733452
Entity Name
NICTAVI
City/State/Country
Los Angeles, CA, US
Establishment Address
1800 Vine Street, Los Angeles, CA 90028, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Nictavi LLC (Owner Number: 10079434)
Owner / Operator Contact Address
1800 Vine Street, Los Angeles, CA 90028, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tarsus Eyelid Patch

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2020-12-06

Official Correspondent

Nathan Horner

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Nictavi LLC
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 3017733452. Last updated year: 2026. Please use registration number 3017733452 when referencing this establishment in official correspondence.
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