Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Osteogenics Biomedical and its 1 subsidiaries with 9 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Jan 23, 2021: Cytoplast Titanium-Reinforced PTFE Membranes.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Osteogenics Biomedical and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 23, 2021 | Cytoplast Titanium-Reinforced PTFE MembranesK201187 · NPK | 510(k) clearances |
| Oct 19, 2017 | RPM Reinforced PTFE MeshK171774 · NPK | 510(k) clearances |
| Sep 7, 2016 | Cytoplast Titanium-Reinforced Posterior Singles Membrane A temporarily implantable material (non-resorbable) for use as a space-making bClass II · The device has the potential to be packaged in the wrong product box. | Device recalls |
| Sep 15, 2015 | VITALA PORCINE DERIVED COLLAGEN MEMBRANEK141177 · NPL | 510(k) clearances |
| Mar 1, 2010 | PRO-FIX PRECISION FIXATION SYSTEM MODEL PFM#, PFB#, PFT#K093719 · DZL | 510(k) clearances |
| Oct 31, 2007 | CYTOPLAST PTFE SUTUREK072076 · NBY | 510(k) clearances |
| May 16, 2002 | IMMIX BONE GRAFT EXTENDERK013764 · KKY | 510(k) clearances |
| Nov 24, 2000 | CYTOPLAST SUTURE; CS-0318, CS-0416, CS-0418, CS-0513, CS-0513PC, CS-0516HCK003028 · NBY | 510(k) clearances |
| Mar 2, 2000 | CYTOPLAST RESORB, MODELS R-250, RP-250, RU-250, RPS-250, RPL-250K993610 · LYC | 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
