MedtechSourcebook

GENESIS DESIGN & FABRICATION

Contract manufacturer ยท Gilbert, AZ

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

FDA registration
3010052529 (openFDA record; or search FDA's registration database)
FEI number
3010052529
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
Genesis Design & Fabrication (FDA owner/operator no. 10043117)
Registered address
1325 W Harwell Rd, Gilbert, AZ 85233
Contract listings
1 device listings, 1 product codes, first listed Jan 25, 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
LXHOrthopedic Manual Surgical InstrumentClass IOrthopedicContract manufacturingJan 25, 2013