ULTRAVIOLET DEVICES, INC.

FDA Device Registration & Listing · VALENCIA, CA, US · Registration 2031894

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
2031894
FEI Number
3001099558
Entity Name
ULTRAVIOLET DEVICES, INC.
City/State/Country
VALENCIA, CA, US
Establishment Address
26145 TECHNOLOGY DR, VALENCIA, CA 91355, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
ULTRAVIOLET DEVICES, INC. (Owner Number: 9035316)
Owner / Operator Contact Address
26145 TECHNOLOGY DR., --, VALENCIA, CA 91355, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

0702-040-000 Smoke Evacuator ULPA Filter 0702-034-000 Fluid Suction HEPA Filter Fluid suction hepa filter Smoke evacuator ulpa/charcoal Fluid suction hepa filter with Carbon hose Fluid suction prefilter

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered General, Plastic Surgery Class 2 878.4780 2015-01-19
FYD Apparatus, Exhaust, Surgical General, Plastic Surgery Class 2 878.5070 2015-01-19
FYD Apparatus, Exhaust, Surgical General, Plastic Surgery Class 2 878.5070 2012-11-28

Official Correspondent

TIM NGO

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ULTRAVIOLET DEVICES, 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
K082762 Aardvark Medical AARDVARK NASAL IRRIGATION AND ASPIRATION DEVICE 2008-11-12

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0038-05 Kinetic Concepts, Inc 2
V.A.C. X-Large Granufoam Dressing Part Numbers M6275065/5, V.A.C. ATS and V.A.C. Freedom and M6275043/5 V.A.C. Classic. Manufactured by Kinetic Concepts, Inc., San Antonio, Texas 78230

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2031894. Last updated year: 2026. Please use registration number 2031894 when referencing this establishment in official correspondence.
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