Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3025431509

FEI Number

3025431509

Entity Name

Mesh Suture, Inc

City/State/Country

Chicago, IL, US

Establishment Address

1444 N Astor St, Ste 3, Chicago, IL 60610, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Mesh Suture, Inc. (Owner Number: 10086760)

Owner / Operator Contact Address

1444 N Astor St, Apt 3, Chicago, IL 60610, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K211178

PMA Number

N/A

All Registered Proprietary Names

Duramesh Mesh Suture

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GAW	Suture, Nonabsorbable, Synthetic, Polypropylene	General, Plastic Surgery	Class 2	878.5010	2022-12-08

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mesh Suture, Inc.

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 3025431509. Last updated year: 2026. Please use registration number 3025431509 when referencing this establishment in official correspondence.