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Anaxdent GmbH

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K112044	ANAXBLEND MODEL 20XXX (SEVERAL), ANAXGUM MODEL 25XXX (U), MOCK-UP DIRECT MODEL 240XXX (U), MOCK-UP DIRECT FLOW MODEL 24A	EBF	2012-01-26	View
510(k)	K023079	NEW OUTLINE	EBG	2002-10-30	View

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