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Osteoremedies, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253675OsteoRemedies Hip Spacer SystemDecember 23, 2025
K250760SPECTRUM GV Bone CementApril 2, 2025
K242377REMEDY Stemmed Knee Spacer System with All-Poly Tibial ComponentOctober 2, 2024
K231556SPECTRUM® GV Bone CementDecember 20, 2023
K223650REMEDY Stemmed Knee SpacerJanuary 5, 2023
K192995OsteoRemedies Hip Spacer SystemJanuary 10, 2020
K191981REMEDY Acetabular CupAugust 23, 2019
K183017Remedy Femoral Component 84mm, Remedy Stemmed Knee SpacerJuly 25, 2019
K172906REMEDY PLUS Hip Spacer, UNITE PLUS Bone CementAugust 29, 2018
K173967Remedy Acetabular CupFebruary 22, 2018
K152267Remedy® Shoulder SpacerDecember 15, 2015