CIRTEC MEDICAL

Contract manufacturer and sterilizer · Brooklyn Park, MN

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

2019Product codes first listed, by year (tallest: 4)2026

FDA registration: 3024996452 (openFDA record; or search FDA's registration database)
FEI number: 3024996452
Registered for: FDA registration year 2026
Establishment types: Contract manufacturer; Contract sterilizer
Owner or operator: Cirtec Medical Corporation (FDA owner/operator no. 10025422)
Registered address: 9315 Winnetka Ave N, Brooklyn Park, MN 55445
Contract listings: 5 device listings, 7 product codes, first listed Oct 18, 2019
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 code	Device (FDA name)	Class	Category	Role	First listed
GWF	Stimulator, Electrical, Evoked Response	Class II	Neurology	Contract manufacturing	Nov 2, 2022
GYC	Electrode, Cortical	Class II	Neurology	Contract manufacturing	Nov 2, 2022
GZF	Stimulator, Peripheral Nerve, Implanted (Pain Relief)	Class II	Neurology	Contract manufacturing	Oct 18, 2019
GZL	Electrode, Depth	Class II	Neurology	Contract manufacturing	Nov 2, 2022
JXE	Device, Nerve Conduction Velocity Measurement	Class II	Neurology	Contract manufacturing	Nov 2, 2022
MNQ	Stimulator, Hypoglossal Nerve, Implanted, Apnea	Class III	Anesthesiology	Contract manufacturing	Aug 18, 2025
MNQ	Stimulator, Hypoglossal Nerve, Implanted, Apnea	Class III	Anesthesiology	Contract sterilization	Aug 18, 2025
QPP	Implantable Post-Surgical Kinematic Measurement Knee Device	Class II	Orthopedic	Contract manufacturing	Sep 7, 2021
QPP	Implantable Post-Surgical Kinematic Measurement Knee Device	Class II	Orthopedic	Contract sterilization	Sep 7, 2021