Omnlife Science
Omnlife Science holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2015.
Top product codes for Omnlife Science
Recent clearances by Omnlife Science
- K142201 — OMNI Interface Acetabular System
- K112779 — APEX MODULAR ACCTABULAR CUP (NOW NAMED APEX INTERFACE ACETABULAR SYSTEM)
- K101994 — APEX KNEE MODULAR TIBIA SYSTEM
- K101575 — APEX MODULAR HEAD, SIZE 28 ,32, 26 AND 40 MM+10.5 OFFSET, MODELS 302810, 303210,303610,304010
- K100151 — APEX HIP SYSTEM BIPOLAR HEAD, MODEL H3-822XX (OD 38 TO 43MM), H3-828XX (OD44 TO 60MM)
- K073602 — MODIFICATION TO: APEX KNEE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.