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Trex Medical Corp.

FDA Regulatory Profile

Trex Medical Corp. has 0 FDA recalls, 0 inspections, 6 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Aug 6, 1999

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances6Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) Clearances

K-NumberDeviceDate
K992229MXU-125 OR TMX-125Aug 6, 1999
K984092PROFILE 2000 MAMMOGRAPHY SYSTEM, PRO-2000Feb 5, 1999
K984091CONTOUR 2000 MAMMOGRAPHY SYSTEM, MODEL CTR- 2000Feb 5, 1999
K984414XRE COLLIMATOR WITH SPECTRAL FILTERDec 30, 1998
K982427TREX TILT C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM, TREX TILT-CSep 23, 1998
K982120DIGITAL IMAGING SYSTEM, MODELS DIGITREX-1000 AND DIGITREX-2000 (DIGITREX-X000 FAMILY)Sep 10, 1998

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.