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4Web, Inc.

USA · Frisco

✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 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

33listed device types

Class I 22Class II 11Class III 0

plus 50 registration records and 13 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

0registered devices

this export covers Class I / II only (the cadastro route)

SASaudi ArabiaSFDA

0registered imported devices

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

CACanadaMDALL

0active device licences

TWTaiwanTFDA

pendingnot queried

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

pendingnot queried

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

pendingnot queried

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 States50 registration records, 13 510(k), 0 PMA, 3 excluded

Manufacturer names merged into this page: 4WEB INC.

FDA 510(k) clearances by year

12014

12015

12016

32017

22018

22019

12020

12021

12026

FDA listed device types

showing 8 of 33

Rod, Fixation, Intramedullary And Accessories 1Appliance, Fixation, Spinal Intervertebral Body 1Pin, Fixation, Smooth 1Intervertebral Fusion Device With Bone Graft, Lumbar 1Intervertebral Fusion Device With Bone Graft, Cervical 1Plate, Fixation, Bone 1Intervertebral Fusion Device With Integrated Fixation, Lumbar 1Screw, Fixation, Bone 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K253201	Lumbar Spine Truss System - Plating Solution (LSTS-PS)	2026-02-12
US	K203065	Lumbar Spine Truss System Plating Solution (LSTS-PS)	2021-03-10
US	K200002	Anterior Spine Truss System Stand Alone (ASTS-SA) Interbody Fusion Device	2020-05-29

4Web, 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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