FirmLabelled 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 Omnlife Science with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jan 26, 2015: OMNI Interface Acetabular System.
| Jan 26, 2015 | OMNI Interface Acetabular SystemK142201 · LPH | 510(k) clearances |
| Dec 2, 2011 | APEX MODULAR ACCTABULAR CUP (NOW NAMED APEX INTERFACE ACETABULAR SYSTEM)K112779 · LPH | 510(k) clearances |
| Sep 28, 2010 | APEX KNEE MODULAR TIBIA SYSTEMK101994 · JWH | 510(k) clearances |
| Jun 30, 2010 | APEX MODULAR HEAD, SIZE 28 ,32, 26 AND 40 MM+10.5 OFFSET, MODELS 302810, 303210,303610,304010K101575 · LPH | 510(k) clearances |
| May 28, 2010 | APEX HIP SYSTEM BIPOLAR HEAD, MODEL H3-822XX (OD 38 TO 43MM), H3-828XX (OD44 TO 60MM)K100151 · KWY | 510(k) clearances |
| Feb 14, 2008 | MODIFICATION TO: APEX KNEE SYSTEMK073602 · JWH | 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
