Buckman Co., Inc.
Buckman Co., Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 1998.
Clearances by Buckman Co., Inc. — page 2
101–111 of 111- K855224 — ACROMED NESTED BONE PLATE
- K852891 — SPINAL FIXATION INSTRUMENTATION SYSTEM
- K851328 — KINETIC AUTO TECHNIC K.A.T. TABLE
- K850142 — ACE INTRAMEDULLARY ROD FOR SMALL BONES
- K841896 — EZ EYE DROP AID
- K843309 — UNIFLEX DANNINGER
- K842768 — ACE/FISHER EXTERNAL FIXATOR
- K842680 — ACE UNIVERSAL TONG
- K834384 — MODULAR EXTREMITY CASTING SUPPORT
- K833866 — ACE/KYLE SELF TAPPING CANNULATED TITA
- K833865 — ACE BROOKER BONE PLATING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.