Omni Life Science, Inc.
Omni Life Science, Inc. holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2019.
Top product codes for Omni Life Science, Inc.
Recent clearances by Omni Life Science, Inc.
- K191765 — OMNI TiN Coated Apex Knee System
- K152919 — OMNI Skirted Heads
- K131472 — APEX KNEE MODULAR TIBIA SYSTEM
- K112891 — APEX REVISION KNEE SYSTEMS
- K113242 — APEX ARC HIP STEM
- K111062 — APEX KNEE SYSTEM, APEX ALL POLY TIBIA
- K111193 — APEX ARC HIP STEM
- K111184 — APEX PS KNEE SYSTEM - PS-C INSERT
- K110947 — APEX K1 HIP STEM
- K102578 — APEX PS KNEE SYSTEM
- K101976 — INTERFACE ACETABULAR SYSTEM, ACETABULAR INSERT +4 OFFSET
- K101451 — APEX MODULE HIP SYSTEM BIOLOX DELTA FEMORAL HEAD
- K090845 — APEX ARC HIP STEM
- K100555 — APEX-LNK ACETABULAR INSERT, E, APEX-LNK ACETABULAR INSERT, F, APEX-LNK
- K094017 — TIBIAL BASEPLATE AUGMENT MODEL KC-22118, KC-22128, KC-22138, KC-22148, KC-22158
- K092443 — INTERFACE ACETABULAR CUP LINERS
- K082468 — APEX HIP SYSTEM BIPOLAR HEAD, MODEL H3-822XX AND H3-828YY, XX=OD IN [MM] (38-43), YY=OD IN [MM](44-60)
- K080842 — APEX KNEE SYSTEM, MODEL KC-230XY, KC-240XY [ NO HOLES, 2 HOLES]
- K073150 — APEX-LNK POLY ACETABULAR CUP LINERS
- K060072 — MONOBLOCK PRESS-FIT HIP STEM
- K060192 — APEX KNEE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.