Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009514842

FEI Number

3009514842

Entity Name

NOVUS SCIENTIFIC INC

City/State/Country

Wrentham, MA, US

Establishment Address

190 Industrial Road, Suite 2, Wrentham, MA 02093, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Novus Scientific (Owner Number: 10046437)

Owner / Operator Contact Address

Virdings Alle 2, Uppsala, SE-C 75450, SE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K191749

PMA Number

N/A

All Registered Proprietary Names

TIGR Matrix Surgical Mesh

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OOD	Surgical Film	General, Plastic Surgery	Class 2	878.3300	2021-02-25
FTL	Mesh, Surgical, Polymeric	General, Plastic Surgery	Class 2	878.3300	2021-02-25
OWT	Mesh, Surgical, Absorbable, Abdominal Hernia	General, Plastic Surgery	Class 2	878.3300	2021-02-25

Official Correspondent

Mona Nessari

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Novus Scientific

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
K220540	Covidien	ProGrip Self-Gripping Polypropylene Mesh	2022-09-22

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009514842. Last updated year: 2026. Please use registration number 3009514842 when referencing this establishment in official correspondence.