Medical Device Manufacturer · FR , Merignac

Satelec - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 1990

24

Total

24

Cleared

0

Denied

FDA 510(k) Regulatory Record - Satelec Dental ✕

21 devices

1-21 of 21

Cleared Dec 08, 2011

Cleared Dec 11, 2009

Cleared Jul 22, 2009

IMPLANT CENTER 2

Cleared Dec 17, 2008

HEMOSTASYL PASTE

Cleared Sep 19, 2007

MINI LED AUTOFOCUS

Cleared Sep 10, 2007

Cleared May 03, 2006

Cleared May 01, 2006

Cleared Jan 25, 2006

BIOSPLINT SPLINTING RIBBON

Cleared Apr 20, 2005

SURPASSON P5 NEWTRON

Cleared Dec 17, 2004

IS 40 MICROMOTOR

Cleared Aug 19, 2004

COCOON HYGIENIST

Cleared Apr 28, 2004

MINI L.E.D. OEM MODULE

Cleared Mar 01, 2004

SP NEWTRON MODULE

Cleared Oct 21, 2003

MINI L.E.D., MODEL: MINI L.E.D., MODEL SMARTLITE MINI

Cleared Jun 07, 2001

TEAM-UP TM DENTAL ELECTRONIC ANESTHESIA SYSTEM

Cleared Apr 04, 2000

Cleared Jul 09, 1997

SP4044 & SP4055 LUX MODULES

Cleared Jul 31, 1996

Cleared May 23, 1996

SUPRASSON P5 BOOSTER

Cleared Sep 29, 1995

SUPRASSON P MAX