ONYX INDUSTRIES, INC.

FDA Device Registration & Listing · GARDENA, CA, US · Registration 2025291

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
2025291
FEI Number
2025291
Entity Name
ONYX INDUSTRIES, INC.
City/State/Country
GARDENA, CA, US
Establishment Address
521 W Rosecrans Ave, GARDENA, CA 90248, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Onyx Industries, Inc. (Owner Number: 2025291)
Owner / Operator Contact Address
521 W. Rosecrans Ave., --, Gardena, CA 90248, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MEDISEPT MEDISEPT STUDEX

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRY Punch, Surgical General, Plastic Surgery Class 1 878.4800 2013-11-26
KAY Punch, Nasal Ear, Nose, Throat Class 1 874.4420 2013-11-14
GDJ Clamp, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2013-11-26
JYS Perforator, Ear-Lobe Ear, Nose, Throat Class 1 874.4420 1992-10-05

Official Correspondent

Leanne Kim

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Onyx Industries, Inc.
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 2025291. Last updated year: 2026. Please use registration number 2025291 when referencing this establishment in official correspondence.
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