Moeller Medical GmbH & Co. KG FDA Record

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

  • No warning letters matched by name
Inspections 0 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 2 Latest Mar 4, 2008

Moeller Medical GmbH & Co. KG has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Moeller Medical GmbH & Co. KG" is on file.

What these totals cover: FDA records filed under the name "Moeller Medical GmbH & Co. KG" and its spelling variant "Moeller Medical Gmbh And Co. Kg". Records filed under related names are not included; see Related names.

Latest 510(k)
Mar 4, 2008

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 11, 2026 (checked Nov 15, 2026, unchanged)File dated Nov 10, 2026Current
510(k) clearances2Nov 15, 2026File dated Nov 9, 2026Current
Inspections0Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent 510(k) clearances

2 510(k) clearances from Aug 25, 2006 to Mar 4, 2008.

K-NumberDeviceDate
K072793LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 688Mar 4, 2008
K053451LIPOSAT (INFILTRATION PUMP), MODEL 00 002 274; VACUSAT (SUCTION UNIT), MODEL 00 002 252 (220 V), 00…Aug 25, 2006

Moeller Medical GmbH & Co. KG and the FDA: common questions

Has Moeller Medical GmbH & Co. KG received an FDA warning letter?

No FDA warning letter addressed to the name "Moeller Medical GmbH & Co. KG" 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 Moeller Medical GmbH & Co. KG received an FDA Form 483?

FDA has not published a Form 483 for "Moeller Medical GmbH & Co. KG" in its reading room. FDA publishes some Form 483s, not all of them.

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