NOVID, LLC

FDA Device Registration & Listing · Oxford, CT, US · Registration 3005178931

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
3005178931
FEI Number
3005178931
Entity Name
NOVID, LLC
City/State/Country
Oxford, CT, US
Establishment Address
115 HURLEY ROAD, UNIT 8D, Oxford, CT 06478, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
NOVID, LLC (Owner Number: 9073584)
Owner / Operator Contact Address
115 HURLEY ROAD, UNIT 8D, Oxford, CT 06478, US
Initial Importer Flag
Y
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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar Orthopedic Class 2 888.3080 2026-02-10

Official Correspondent

DAVID BURKHART

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NOVID, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K192492 Astura Medical, LLC EL CAPITAN Anterior Lumber Interbody System 2020-04-21
K212498 Nexus Spine, LLC Stable-L Standalone Lumbar Interbody System 2022-03-18

Similar Registrations

Registration Number Establishment Name Location
3017936978 CARLSMED, INC. Carlsbad, CA, US
3016050940 Olive Branch Distribution Center Olive Branch, MS, US
3006783837 STRUCTURE MEDICAL, LLC. Naples, FL, US
3011795235 MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH DEGGENDORF Bavaria, DE
1424263 Isomedix Operations, Inc. Libertyville, IL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005178931. Last updated year: 2026. Please use registration number 3005178931 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.