MedtechSourcebook

PICOCYL

Contract manufacturer ยท Golden, CO

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

2022Product codes first listed, by year (tallest: 2)2026
FDA registration
3015176914 (openFDA record; or search FDA's registration database)
FEI number
3015176914
Registered for
FDA registration year 2026
Establishment types
Complaint file establishment; Contract manufacturer; Repackager or relabeler
Owner or operator
PICOCYL (FDA owner/operator no. 10085594)
Registered address
150 CAPITAL DRIVE, STE. 470, Golden, CO 80401
Contract listings
2 device listings, 2 product codes, first listed Dec 9, 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
FMINeedle, Hypodermic, Single LumenClass IIGeneral hospitalContract manufacturingDec 9, 2022
GAANeedle, Aspiration And Injection, DisposableClass IGeneral and plastic surgeryContract manufacturingDec 9, 2022

Other contract facilities of PICOCYL