Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016648678

FEI Number

3016648678

Entity Name

INNOVERO, LLC

City/State/Country

Colorado Springs, CO, US

Establishment Address

629 Elkton Drive, Unit B, Colorado Springs, CO 80907, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

InnoVero, LLC (Owner Number: 10062515)

Owner / Operator Contact Address

629 Elkton Drive, Unit B, Colorado Springs, CO 80907, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNI	Container, Specimen, Non-Sterile	Pathology	Class 1	864.3250	2020-03-24

Official Correspondent

Gabriel Baida

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

InnoVero, LLC

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 3016648678. Last updated year: 2026. Please use registration number 3016648678 when referencing this establishment in official correspondence.