Home / Device Classification / EIX

EIX — Probe, Periodontic Class I

FDA Device Classification

Classification Details

Product Code
EIX
Device Class
Class I
Regulation Number
872.4565
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K960245pro-dentecVIP VICTOR INTERACTIVE PROBEApril 4, 1996
K944848rms divTHE VIVACARE T.P.S. PROBEDecember 14, 1994
K936221pd internationalPROBE TIP/PERI PROBE/PERI PROBE COMP.August 1, 1994
K890333alpkemALBUMIN REAGENTFebruary 17, 1989
K880827sweet micro systemsACCUTEK PERIODONTAL PROBEApril 12, 1988
K875076florida probeFLORIDA PROBEMarch 10, 1988
K870280accudentACCUDENT ACCUPROBEJune 8, 1987
K871504periodontal health brushDISPOSABLE PERIODONTAL PROBEMay 6, 1987
K823324miltexDENTAL INSTRUMENTS - PROBESNovember 24, 1982