Jiangsu Trausim Medical Instrument FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Jiangsu Trausim Medical Instrument has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Jiangsu Trausim Medical Instrument" is on file.

What these totals cover: FDA records filed under the name "Jiangsu Trausim Medical Instrument".

Latest 510(k)
Dec 12, 2014

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances1Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent 510(k) clearances

1 510(k) clearance on Dec 12, 2014.

K-NumberDeviceDate
K140202TRAUSIM DENTAL IMPLANT SYSTEMDec 12, 2014

Jiangsu Trausim Medical Instrument and the FDA: common questions

Has Jiangsu Trausim Medical Instrument received an FDA warning letter?

No FDA warning letter addressed to the name "Jiangsu Trausim Medical Instrument" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Jiangsu Trausim Medical Instrument received an FDA Form 483?

FDA has not published a Form 483 for "Jiangsu Trausim Medical Instrument" in its reading room. FDA publishes some Form 483s, not all of them.

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