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Davis Schottlander & Davis, Ltd.

FDA Regulatory Profile

Davis Schottlander & Davis, Ltd. has 0 FDA recalls, 2 inspections, 7 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 24, 2015 · VAI
Latest 510(k)
Jan 22, 2004

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances7Oct 4, 2026Not statedCurrent
Inspections2Oct 27, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 24, 2015Letchworth Garden City, United KingdomDevicesVoluntary Action Indicated (VAI)1000269600
Jun 3, 2010Letchworth Garden City, United KingdomDevicesVoluntary Action Indicated (VAI)1000269600

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K024252MATCH MASTER LOW FUSION PORCELAINJan 22, 2004
K024250MATCH PRESS PRESSABLE CERAMICAug 25, 2003
K001463SCHOTTLANDER ENIGMA COLOUR TONE, MODEL 0156Jun 16, 2000
K993717ENIGMA HI-BASE DENTURE BASE MATERIALDec 22, 1999
K984134NATURA DENTURE TEETHFeb 12, 1999
K984128ENIGMA DENTURE TEETHFeb 9, 1999
K960770MATCHMAKER/PROPAQUE PORCELAINNov 19, 1996

FDA data resources