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Medline Industries, Inc.

USA · Northfield

✓ Record-verifiedregistrations found in 9 markets

This company has registrations in United States, Brazil, Saudi Arabia, Canada, Singapore, South Korea, Australia, Hong Kong, Israel — 9 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable

CNChinaNMPA

n/aThis registry lists domestic registrants only

EUEuropean UnionEUDAMED

pendingnot queried

USUnited StatesFDA openFDA

753listed device types

Class I 487Class II 246Class III 5unclassified 15

plus 1,548 registration records and 275 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

179registered devices

Class I 150Class II 29

184 including historic records

SASaudi ArabiaSFDA

64registered imported devices

low-risk imported devices only; a 2023 snapshot, not updated since

CACanadaMDALL

141active device licences

Class II 139Class III 1Class IV 1

500 including historic records

TWTaiwanTFDA

0valid device licences

SGSingaporeHSA SMDR

20device registrations

CLASS B 20

KRSouth KoreaMFDS GMP

2GMP quality-system certificates

Import 2

AUAustraliaTGA ARTG

50active ARTG entries

Class I 20IIa 18IIb 2Class Im (measuring) 1Class Is (sterile) 9

HKHong KongMDACS

1valid listings

Class II 1

ILIsraelAMAR

9registrations

RURussiaRoszdravnadzor

pendingnot queried

Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States1,548 registration records, 275 510(k), 0 PMA, 19 excluded

Brazil179 confirmed, 8 excluded

Saudi Arabia64 confirmed, 0 excluded

Canada141 confirmed, 2 excluded

Manufacturer names merged into this page: MEDLINE INDUSTRIES, LP - Laredo · Medline Industries, LP - Mexicali (MXC) · MEDLINE INDUSTRIES, LP (Northpoint Services) · MEDLINE INDUSTRIES, LP - SPT · MEDLINE INDUSTRIES, LP · MEDLINE INDUSTRIES, INC

FDA 510(k) clearances by year

12007

52008

12009

42010

102011

42012

52013

42014

102015

112016

72017

112018

112019

202020

92021

122022

102023

122024

52025

42026

FDA listed device types

showing 8 of 753

Electrosurgical, Cutting & Coagulation & Accessories 1Spirometer, Therapeutic (Incentive) 1Forceps, Surgical, Gynecological 1Cystoscope And Accessories, Flexible/Rigid 1Mesh, Surgical, Non-Absorbable, Orthopaedics, Reinforcement Of Tendon 1Gown, Non-Sterile, Non-Isolation, Intended To Provide Moderate Or High Barrier Protection 1Needle, Conduction, Anesthetic (W/Wo Introducer) 1Probe, Blood-Flow, Extravascular 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K253526	NAMIC Dilator and Sheath	2026-07-29
US	K254287	Medline Reusable Blood Pressure Cuff	2026-06-22
US	K253322	Hudson RCI® Infant Dri-TechTM Breathing Circuits (HUD99060 / Dri-Tech with 78 Infant Circuit, HUD99060KIT / Dri-Tech with 78 Infant Circuit Kit, HUD99001KIT / Single Limb Infant Circuit Dri-Tech Kit, HUD99009KIT / Dri-Tech with 60 Infant Circuit Kit, HUD99018KIT / Dri-Tech with 44 Infant Circuit Kit, HUD870NKIT / Dri-Tech Infant Accessory Bag, HUD1631 / Infant Wye Connector with Swivel)	2026-03-25
BR	80170310055	CAMPO CIRÚRGICO DESCARTÁVEL PROXIMA	Class I
BR	80170310055	CAMPO CIRÚRGICO DESCARTÁVEL PROXIMA	Class I
BR	80170310055	CAMPO CIRÚRGICO DESCARTÁVEL PROXIMA	Class I
SA	ME0000005304SFDAA00001	Bouffant Caps	—
SA	ME0000005304SFDAA00002	Cover Gowns	—
CA	3304	VINYL MEDICAL EXAMINATION GLOVES	Class II
CA	3377	NECESSAIRE A PANSEMENT AVEC ANTISEPTIQUE PVP.	Class II
CA	3429	NON-LATEX POWDER FREE SURGICAL GLOVES, STERILE	Class II

Medline Industries, Inc.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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