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Tautona Group, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K242536TauTona Pneumoperitoneum Assist Device (TPAD)October 15, 2024
K131963TAUTONA INJECTOR DEVICEOctober 22, 2013