Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Osteoremedies, LLC with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jul 24, 2026: REMEDY POLY+PLUS SNAP FIT Acetabular Cup.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jul 24, 2026 | REMEDY POLY+PLUS SNAP FIT Acetabular CupK262290 · KWL | 510(k) clearances |
| Dec 23, 2025 | OsteoRemedies Hip Spacer SystemK253675 · KWL | 510(k) clearances |
| Apr 2, 2025 | SPECTRUM GV Bone CementK250760 · LOD | 510(k) clearances |
| Oct 2, 2024 | REMEDY Stemmed Knee Spacer System with All-Poly Tibial ComponentK242377 · JWH | 510(k) clearances |
| Dec 20, 2023 | SPECTRUM® GV Bone CementK231556 · LOD | 510(k) clearances |
| Jan 5, 2023 | REMEDY Stemmed Knee SpacerK223650 · JWH | 510(k) clearances |
| Jan 10, 2020 | OsteoRemedies Hip Spacer SystemK192995 · KWL | 510(k) clearances |
| Aug 23, 2019 | REMEDY Acetabular CupK191981 · KWL | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
