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.

Aesculap-Meditec North America

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K994116	LASER SYSTEM MEDIOSTAR H (WITH AND WITHOUT SKIN COOLING SYSTEM)	GEX	2000-06-01	View
510(k)	K992707	MCL 29 DERMABLATE ER:YAG LASER SYSTEM	GEX	1999-10-19	View
510(k)	K991285	LASER SYSTEM RUBYSTAR WITH Q-SWITCH AND NORMAL MODE	GEX	1999-07-12	View
510(k)	K981196	MEDITEC LINK	HQF	1998-06-17	View
510(k)	K980361	DERMABLATE ER: YAG LASER SYSTEM	GEX	1998-04-21	View
510(k)	K974467	AESCULAP-MEDITEC SLIT LAMPS SL07 AND SL08	HJO	1998-02-19	View

↑