MedtechSourcebook

PHAMATECH INC.

Contract manufacturer ยท San Diego, CA

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

2007Product codes first listed, by year (tallest: 1)2026
FDA registration
2031229 (openFDA record; or search FDA's registration database)
FEI number
3000719950
Registered for
FDA registration year 2026
Establishment types
Specification developer; Manufacturer for export only; Manufacturer; Contract manufacturer; Repackager or relabeler
Owner or operator
PHAMATECH INC. (FDA owner/operator no. 9026390)
Registered address
15175 Innovation Dr, San Diego, CA 92128
Contract listings
2 device listings, 2 product codes, first listed May 7, 2007
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
LCXKit, Test, Pregnancy, Hcg, Over The CounterClass IIClinical chemistryContract manufacturingMay 7, 2007
QKOReagent, Coronavirus SerologicalNot classifiedMicrobiologyContract manufacturingMar 20, 2020