VERO BIOTECH INC.

FDA Device Registration & Listing · Livingston, TN, US · Registration 3012160128

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3012160128
FEI Number
3012160128
Entity Name
VERO BIOTECH INC.
City/State/Country
Livingston, TN, US
Establishment Address
208 N Main St, Livingston, TN 38570, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Vero Biotech Inc. (Owner Number: 10095885)
Owner / Operator Contact Address
387 Nerem St NW, Suite 125, Atlanta, GA 30313, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

NOxBOXi System Patient Kits

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MRN Apparatus, Nitric Oxide Delivery Anesthesiology Class 2 868.5165 2026-05-15

Official Correspondent

Megan Bevill

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vero Biotech Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0028-2026 NOXBOX LTD 2
NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I
Z-0029-2026 NOXBOX LTD 2
NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012160128. Last updated year: 2026. Please use registration number 3012160128 when referencing this establishment in official correspondence.
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