Medical device makerLabelled 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 15, 2026, FDA's public records list Science for Biomaterials with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jun 3, 2014: OTIS-C-PLUS, NEOTIS PLATE, SCREW 06.5.
| Jun 3, 2014 | OTIS-C-PLUS, NEOTIS PLATE, SCREW 06.5K140226 · HRS | 510(k) clearances |
| Apr 19, 2012 | OTIS-C PLUSK120818 · HRS | 510(k) clearances |
| May 6, 2009 | LIGAFIX INTERFACE SCREWK090994 · HWC | 510(k) clearances |
| Jul 3, 2007 | MODIFICATION TO: BIOSORB RESORBABLE VOID FILLERK071155 · MQV | 510(k) clearances |
| Mar 29, 2007 | MODIFICATION TO: LIGAFIX INTERFERENCE SCREWK070507 · HWC | 510(k) clearances |
| May 24, 2006 | BIO 1-KIT BIOSORB FILLED CARTRIDGEK061022 · MQV | 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
