MedtechSourcebook

HI-TECH PRODUCTS INC.

Contract manufacturer ยท Buena Park, CA

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

2013Product codes first listed, by year (tallest: 2)2026
FDA registration
2030616 (openFDA record; or search FDA's registration database)
FEI number
3000207077
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
Hi-Tech Products Inc. (FDA owner/operator no. 10045089)
Registered address
8530 Roland St, Buena Park, CA 90621
Contract listings
5 device listings, 5 product codes, first listed Oct 21, 2013
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
HOYShield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)Class IOphthalmicContract manufacturingOct 27, 2021
JOJIndicator, Physical/Chemical Sterilization ProcessClass IIGeneral hospitalContract manufacturingJul 22, 2016
KGXTape And Bandage, AdhesiveClass IGeneral hospitalContract manufacturingOct 30, 2013
MNGExternal Urethral Occluder, Urinary Incontinence-Control, FemaleClass IGastroenterology and urologyContract manufacturingJun 7, 2018
NACDressing, Wound, HydrophilicClass IGeneral and plastic surgeryContract manufacturingOct 21, 2013