HEXIRIS, INC.

FDA Device Registration & Listing · Dieppe New Brunswick, CA · Registration 3040185492

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
3040185492
FEI Number
3040185492
Entity Name
HEXIRIS, INC.
City/State/Country
Dieppe New Brunswick, CA
Establishment Address
5085 Principale-Est Ave, Dieppe New Brunswick E1A9T8, CA
Establishment Type(s)
Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Hexiris, Inc. (Owner Number: 10093887)
Owner / Operator Contact Address
5085 Principale-Est Ave, Dieppe, CA-NB E1A9T8, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HNJ Punch, Corneo-Scleral Ophthalmic Class 1 886.4350 2025-07-29

Official Correspondent

Ken Johannaber

US Agent Details

Ken Johannaber Email: ken@cieodesign.com Phone: (916) 4791474

Related Public Records

Same Entity

Hexiris, 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
K871646 Ocular Instruments, Inc. TANNE CORNEAL CUTTING BLOCK 1987-05-18

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3040185492. Last updated year: 2026. Please use registration number 3040185492 when referencing this establishment in official correspondence.
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