Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Mednext, Inc.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K983092	TRITON HUDSON CHUCK ATTACHMENT	HBB	1998-11-06	View
510(k)	K972308	MEDNEXT 1000 DRILL	GEY	1997-08-20	View
510(k)	K970023	MEDNEXT SURGICAL BUR	HWE	1997-02-28	View
510(k)	K943108	MEDNEXT MICRO-DRILL	ERL	1994-08-17	View
510(k)	K935861	MEDNEXT BUR	HBE	1994-05-03	View
510(k)	K935584	MEDNEXT BUR	EQJ	1994-02-22	View
510(k)	K926547	MEDNEXT 1000 BONE DISSECTING SYSTEM	HSZ	1993-07-22	View

↑