Bowen & Company, Inc.
Bowen & Company, Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1990.
Top product codes for Bowen & Company, Inc.
Recent clearances by Bowen & Company, Inc.
- K896898 — BOWEN ELECTRODE SKIN PREPATORY CLEANSER
- K896538 — DISPOSABLE 45 DEGREE SHAVER
- K873766 — STERNAL POWER AWL
- K872098 — CREMEEN ALVEOLAR BONE CALIPER
- K871325 — BOWEN REUSEABLE/DISPOSABLE ELECTRODE
- K870881 — LOOSE BODY GRASPERS
- K870882 — 45 DEGREE SHAVER
- K863146 — BOWEN SUTURE PASSER
- K863147 — GLENOID DRILL
- K863148 — BOWEN KNOT PASSER
- K863149 — BOWEN PROBE
- K863150 — BOWEN CANNULA
- K853376 — MORGAN SUTURE-DRILL
- K853601 — MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP
Data sourced from openFDA. This site is unofficial and independent of the FDA.