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Anx Robotica Corporation

USA · Plano

✓ 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

6listed device types

Class I 0Class II 6Class III 0

plus 12 registration records and 10 510(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 States12 registration records, 10 510(k), 0 PMA

Manufacturer names merged into this page: ANX ROBOTICA CORP.

FDA 510(k) clearances by year

12019

22020

12021

12022

22023

22024

12025

FDA listed device types

System, Imaging, Gastrointestinal, Wireless, Capsule 1Gastrointestinal Motility System, Capsule 1System, Gastrointestinal Motility (Electrical) 1Tether Accessory For Use In The Gastrointestinal Tract 1Gastrointestinal Capsule Endoscopy Analysis Software Device 1Magnetically Maneuvered Capsule Endoscopy System 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K250493	MotiliCap GI Monitoring System	2025-05-21
US	K241934	NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach Capsule/Tether (NaviCam Xpress Stomach System with NaviCam Capsule/Tether)	2024-07-31
US	K233229	NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB Capsule and NaviCam Tether	2024-01-05

Anx Robotica Corporation

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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