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Lorad, A Hologic Co.

FDA Regulatory Profile

Lorad, A Hologic Co. has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jan 11, 2013

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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) clearances5Oct 4, 2026Not statedCurrent
Inspections0Oct 23, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K122836AFFIRM BREAST BIOPSY GUIDANCE SYSTEMJan 11, 2013
K071542DIGITAL STEREOLOC IIJul 5, 2007
K030666MULTICARE PLATINUM SYSTEM AND ACCESSORIESMar 25, 2003
K013290MODIFIED 650 MAMMOGRAPHY SYSTEMOct 24, 2001
K011987MODIFIED M-IV MAMMOGRAPHY SYSTEMJul 11, 2001

FDA data resources