Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013668043

FEI Number

3013668043

Entity Name

CONFLUENT MEDICAL TECHNOLOGIES, INC.

City/State/Country

Warwick, RI, US

Establishment Address

60 Commerce Drive, Warwick, RI 02886, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Confluent Medical Technologies, Inc. (Owner Number: 10033958)

Owner / Operator Contact Address

6263 N. Scottsdale Road, Suite 224, Scottsdale, AZ 85250, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DYNATAPE Suture PERMATAPE Suture ACTIVBRAID MaxBraid BroadBand Suture And Expressbraid BroadBand Graft Manipulation Suture

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GAT	Suture, Nonabsorbable, Synthetic, Polyethylene	General, Plastic Surgery	Class 2	878.5000	2026-06-18
GAT	Suture, Nonabsorbable, Synthetic, Polyethylene	General, Plastic Surgery	Class 2	878.5000	2025-04-08
GAT	Suture, Nonabsorbable, Synthetic, Polyethylene	General, Plastic Surgery	Class 2	878.5000	2024-05-09
GAT	Suture, Nonabsorbable, Synthetic, Polyethylene	General, Plastic Surgery	Class 2	878.5000	2020-01-07

Official Correspondent

Rich Brown

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Confluent Medical Technologies, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3007635982	Confluent Medical Technologies, Inc	Fremont, CA, US
3009018440	Nitinol Devices & Components Costa Rica, S. R. L.	El Coyol Alajuela, CR

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K072322	Smith & Nephew, Inc.	ULTRA FAST-FIX AND ULTRA FAST-FIX AB MENISCAL REPAIR SYSTEMS	2007-09-18

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013668043. Last updated year: 2026. Please use registration number 3013668043 when referencing this establishment in official correspondence.