ClearanceBrief
Company · US

Osteoremedies, LLC

FDA 510(k) clearances and medical device recalls filed under this name, 2015 to 2026. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (2 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KWLProsthesis, Hip, Hemi-, Femoral, Metal6
JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer3
LODBone Cement2
KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 24, 2026K262290REMEDY POLY+PLUS SNAP FIT Acetabular Cup
Osteoremedies, LLC
KWL
Dec 23, 2025K253675OsteoRemedies Hip Spacer System
Osteoremedies, LLC
KWL
Apr 2, 2025K250760SPECTRUM GV Bone Cement
Osteoremedies, LLC
LOD
Oct 2, 2024K242377REMEDY Stemmed Knee Spacer System with All-Poly Tibial Component
Osteoremedies, LLC
JWH
Dec 20, 2023K231556SPECTRUM® GV Bone Cement
Osteoremedies, LLC
LOD
Jan 5, 2023K223650REMEDY Stemmed Knee Spacer
Osteoremedies, LLC
JWH
Jan 10, 2020K192995OsteoRemedies Hip Spacer System
Osteoremedies, LLC
KWL
Aug 23, 2019K191981REMEDY Acetabular Cup
Osteoremedies, LLC
KWL
Jul 25, 2019K183017Remedy Femoral Component 84mm, Remedy Stemmed Knee Spacer
Osteoremedies, LLC
JWH
Aug 29, 2018K172906REMEDY PLUS Hip Spacer, UNITE PLUS Bone Cement
Osteoremedies, LLC
KWL
Feb 22, 2018K173967Remedy Acetabular Cup
Osteoremedies, LLC
KWL
Dec 15, 2015K152267Remedy® Shoulder Spacer
Osteoremedies, LLC
KWS

Latest recalls

DateFirm and productCodeLinked 510(k)
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