Omni Life Science, Inc.
FDA 510(k) medical device clearances.
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.