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Company · US

Aribex, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2017. Name variants (Inc, Corp, punctuation) are merged.

4510(k) clearances (0 in 12 months)

2recalls (0 in 12 months)

2recalls that name a 510(k)

Product codes

Code	Device	Records
EHD	Unit, X-Ray, Extraoral With Timer	5
IZL	System, X-Ray, Mobile	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Nov 16, 2017	K173319	KaVo NOMAD Pro 2 Handheld X-ray System Aribex	EHD
Aug 19, 2014	K140723	NOMAD MD 75K V HANDHELD X-RAY SYSTEM Aribex, Inc.	IZL
Jun 23, 2008	K081664	NOMAD PRO X-RAY SYSTEM Aribex, Inc.	EHD
Jul 14, 2005	K051795	NOMAD DENTAL X-RAY SYSTEM Aribex, Inc.	EHD

Latest recalls

Date	Firm and product	Code	Linked 510(k)
Sep 2, 2016	Aribex Inc NOMAD Pro2 Packaged X-Ray System, Part Number 08500021; NOMAD Pro2 Packaged X-Ray System Black, Part Number 08500022; NOMAD Pro2 Vet Packaged X-Ray System, Part Number 08500023; NOMAD Pro2 Vet Package Terminated	EHD	K081664
Sep 2, 2016	Aribex Inc NOMAD Pro Packaged X-Ray System, Part Number 08500009; NOMAD Pro Vet Packaged X-Ray System, Part Number 08500011; NOMAD Pro Packaged X-Ray System - Europe, Part Number 08500013; NOMAD Pro X-Ray System Terminated	EHD	K081664

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