Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015176914

FEI Number

3015176914

Entity Name

PICOCYL

City/State/Country

Golden, CO, US

Establishment Address

150 CAPITAL DRIVE, STE. 470, Golden, CO 80401, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device

Owner / Operator

PICOCYL (Owner Number: 10085594)

Owner / Operator Contact Address

150 CAPITAL DRIVE, STE. 470, Golden, CO 80401, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Self Administration Support Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OJV	Single Use Instrument Tray	General, Plastic Surgery	Class 1	878.4800	2025-07-21

Official Correspondent

Gary Holland

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PICOCYL

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3043531632	Picocyl	Golden, CO, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015176914. Last updated year: 2026. Please use registration number 3015176914 when referencing this establishment in official correspondence.