Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010187263

FEI Number

3010187263

Entity Name

NOVUS SCIENTIFIC AB

City/State/Country

Uppsala, SE

Establishment Address

Virdings Alle 2, Uppsala 754 50, SE

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Novus Scientific AB (Owner Number: 10034484)

Owner / Operator Contact Address

Virdings Alle 2, Uppsala, SE-C 754 50, 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	2021-12-17
OWT	Mesh, Surgical, Absorbable, Abdominal Hernia	General, Plastic Surgery	Class 2	878.3300	2021-12-17
FTL	Mesh, Surgical, Polymeric	General, Plastic Surgery	Class 2	878.3300	2021-12-17

Official Correspondent

Mona Nessari

US Agent Details

William Barrett Business: Global medical Partners Email: bbarrett@globalmedllc.com Phone: (888) 3848490

Related Public Records

Same Entity

Novus Scientific AB

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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3005670760	Tepha, Incorporated	Lexington, MA, US
3009337401	Synergy Health Ede BV	Venlo Limburg, NL

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010187263. Last updated year: 2026. Please use registration number 3010187263 when referencing this establishment in official correspondence.