MedtechSourcebook

Aprios Custom Mfg.

Contract manufacturer ยท Minneapolis, MN

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

2022Product codes first listed, by year (tallest: 3)2026
FDA registration
3004612223 (openFDA record; or search FDA's registration database)
FEI number
3004612223
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
Diversified Plastics, Inc (FDA owner/operator no. 10043677)
Registered address
8617 Xylon Ct, Minneapolis, MN 55445
Contract listings
4 device listings, 5 product codes, first listed Jul 25, 2022
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
EOBNasopharyngoscope (Flexible Or Rigid)Class IIEar, nose and throatContract manufacturingApr 25, 2026
JRLUnit, Filter, MembraneClass IClinical chemistryContract manufacturingFeb 6, 2024
OTNMesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or TransobturatorClass IIGeneral and plastic surgeryContract manufacturingApr 25, 2026
PAHMesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Female, Mini-SlingClass IIGeneral and plastic surgeryContract manufacturingApr 25, 2026
PBQFixation, Non-Absorbable Or Absorbable, For Pelvic UseClass IIObstetrics and gynecologyContract manufacturingJul 25, 2022