Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010119152

FEI Number

3010119152

Entity Name

PINNACLE BIOLOGICS, INC.

City/State/Country

Bannockburn, IL, US

Establishment Address

2801 Lakeside Drive, Suite 210, Bannockburn, IL 60015, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Advanz Pharma (US) Corp. (Owner Number: 10043852)

Owner / Operator Contact Address

2801 Lakeside Drive, Ste 210, Office 7, Bannockburn, IL 60015, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P990021

All Registered Proprietary Names

OPTIGUIDE FIBER OPTIC DIFFUSER DIOMED 630 PDT LASER ANGIO DYNAMICS 630PDT LASER PHOTOFRIN 630 PDT LASER; MODEL 63012

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MVG	System, Laser, Fiber Optic, Photodynamic Therapy	Unknown	Class 3	N/A	2013-03-28
MVF	System, Laser, Photodynamic Therapy	Unknown	Class 3	N/A	2013-03-28

Official Correspondent

Larry Miles

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Advanz Pharma (US) Corp.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010119152. Last updated year: 2026. Please use registration number 3010119152 when referencing this establishment in official correspondence.