MedtechSourcebook

PROMED PHARMA

Contract manufacturer ยท Plymouth, MN

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

2013Product codes first listed, by year (tallest: 4)2026
FDA registration
3003335547 (openFDA record; or search FDA's registration database)
FEI number
3003335547
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
ProMed Pharma (FDA owner/operator no. 10042894)
Registered address
15600 Medina Rd, Plymouth, MN 55447
Contract listings
4 device listings, 7 product codes, first listed Jan 9, 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
LGWStimulator, Spinal-Cord, Totally Implanted For Pain ReliefClass IIINeurologyContract manufacturingApr 12, 2022
MHYStimulator, Electrical, Implanted, For Parkinsonian TremorClass IIINeurologyContract manufacturingApr 12, 2022
NHLStimulator, Electrical, Implanted, For Parkinsonian SymptomsClass IIINeurologyContract manufacturingApr 12, 2022
NZCStent, Urethral, Prostatic, Semi-PermanentClass IIIGastroenterology and urologyContract manufacturingJan 9, 2013
PJSStimulator, Electrical, Implanted, For Essential TremorClass IIINeurologyContract manufacturingApr 12, 2022
QCDContinuous Glucose Monitor, Implanted, Adjunctive UseClass IIIClinical chemistryContract manufacturingFeb 29, 2024
QHJSensor, Glucose, Implanted, Non-Adjunctive UseClass IIIClinical chemistryContract manufacturingFeb 29, 2024