Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Buckman Co., Inc. — Predicate Candidate Screening
111 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
64 daysmedian FDA review time
287 days90th percentile
111clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K961320 | CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS | Buckman Co., Inc. | 1998-06-25 | 811 | 0 |
| K974641 | FUTURELASE 3000/3002 ERBIUM LASER SYSTEM | Buckman Co., Inc. | 1998-06-08 | 175 | 0 |
| K964252 | ORTHOCHUCK | Buckman Co., Inc. | 1997-05-27 | 215 | 0 |
| K950099 | SYNERGY(TM) TI POSTERIOR SPINAL SYSTEM | Buckman Co., Inc. | 1997-01-16 | 737 | 0 |
| K960451 | WEBB-MORLEY SPINE SYSTEM | Buckman Co., Inc. | 1996-04-18 | 79 | 0 |
| K950999 | KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS | Buckman Co., Inc. | 1996-01-25 | 328 | 0 |
| K945756 | IMAGN(TM) 2000 SYSTEM | Buckman Co., Inc. | 1995-12-19 | 391 | 0 |
| K940003 | VOLUMET CD4 + AND CD8 + T LYMPHOCYTE COUNT TEST KIT | Buckman Co., Inc. | 1995-10-19 | 654 | 0 |
| K951117 | LIHTAN 532 LASER | Buckman Co., Inc. | 1995-10-18 | 222 | 0 |
| K942751 | VANGUARD SERIES GAS REGULATORS | Buckman Co., Inc. | 1995-02-09 | 244 | 0 |
| K934429 | ANTERIOR SPINE SYSTEM | Buckman Co., Inc. | 1994-10-20 | 402 | 0 |
| K931778 | LAPAROSCOPY INSTRUMENTS | Buckman Co., Inc. | 1994-04-12 | 368 | 0 |
| K921686 | ENDOMED LAPAROSCOPY INSTRUMENTS | Buckman Co., Inc. | 1994-03-30 | 721 | 0 |
| K935950 | FX-CABLELOK CABLE/PLATE SYSTEM | Buckman Co., Inc. | 1994-03-09 | 86 | 0 |
| K932723 | CONBIO CUB-D10 COPPER LASER SYSTEM | Buckman Co., Inc. | 1994-02-03 | 244 | 0 |
| K930634 | SUR FLO THERMAL THERAPY PADS | Buckman Co., Inc. | 1993-11-01 | 266 | 0 |
| K921056 | COTREL - DUBOUSSET SPINE IMPLANTS | Buckman Co., Inc. | 1993-06-24 | 476 | 0 |
| K921767 | COMPACT COTREL -- DUBOUSSET SPINE SYSTEM | Buckman Co., Inc. | 1993-06-22 | 434 | 0 |
| K922935 | CONBIO-MEDLITE Q-SWITCHED ND:YAG LASER SYSTEM | Buckman Co., Inc. | 1993-04-07 | 293 | 0 |
| K922919 | DYNACYT BIOPSY ASPIRATION DEVICE | Buckman Co., Inc. | 1993-03-31 | 287 | 0 |
| K924484 | ARTROMOT MULTI DIRECTIONAL ANKLE CPM | Buckman Co., Inc. | 1993-03-22 | 200 | 0 |
| K923857 | ARTROMOT SB ELBOW ATTACHMENT | Buckman Co., Inc. | 1993-02-12 | 196 | 0 |
| K922901 | INCISOR I PULSED ND:YAG LASER SYSTEM | Buckman Co., Inc. | 1992-11-20 | 157 | 0 |
| K923217 | DANNIFLEX CPM 2000 | Buckman Co., Inc. | 1992-08-03 | 33 | 0 |
| K923216 | DANNINFLEX CPM 800 | Buckman Co., Inc. | 1992-08-03 | 33 | 0 |
| K912931 | ITM SONIC SURGERY SYSTEM | Buckman Co., Inc. | 1991-10-03 | 90 | 0 |
| K904505 | CCI CORNEAL SCARIFIER | Buckman Co., Inc. | 1991-04-23 | 203 | 0 |
| K904735 | DANNIFLEX MODEL 500TM CPM | Buckman Co., Inc. | 1991-01-30 | 105 | 0 |
| K902525 | ACE/WILLIAMS MICROSURGERY SAW SYSTEM | Buckman Co., Inc. | 1990-11-26 | 174 | 0 |
| K900264 | R-BAND(TM) RESPIRATORY SENSOR | Buckman Co., Inc. | 1990-07-24 | 187 | 0 |
| K901984 | ACE WIRE TENSION CLAMP | Buckman Co., Inc. | 1990-06-21 | 50 | 0 |
| K896634 | CARAGLAS XTRA SYNTHETIC CASTING TAPE | Buckman Co., Inc. | 1990-06-14 | 204 | 0 |
| K901677 | CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTER | Buckman Co., Inc. | 1990-04-23 | 13 | 0 |
| K900581 | DANNIFLEX CPM 880(TM) | Buckman Co., Inc. | 1990-02-20 | 13 | 0 |
| K894982 | ACE WIRE TENSION CLAMP | Buckman Co., Inc. | 1990-01-11 | 156 | 0 |
| K896044 | CROSS CANCELLOUS BONE SCREW | Buckman Co., Inc. | 1989-11-09 | 23 | 0 |
| K893928 | LEVTECH SMALL BONE PLATE | Buckman Co., Inc. | 1989-11-03 | 156 | 0 |
| K894472 | CROSS ROUND & SQUARE SPINAL RODS & DIST. SPINAL | Buckman Co., Inc. | 1989-10-10 | 84 | 0 |
| K895079 | ACE BEADED K-WIRES ACE OLIVE WIRES | Buckman Co., Inc. | 1989-09-13 | 30 | 0 |
| K895015 | ARTROMOT(TM) CPM DEVICES | Buckman Co., Inc. | 1989-09-11 | 34 | 0 |
| K895107 | ACE ORTHOPAEDIC WASHERS | Buckman Co., Inc. | 1989-09-11 | 27 | 0 |
| K891405 | BMS-2000 MOBILE EEG SYSTEM | Buckman Co., Inc. | 1989-08-02 | 141 | 1 |
| K884161 | ACROMED ILIAC SCREW | Buckman Co., Inc. | 1989-05-03 | 211 | 0 |
| K884163 | ACROMED SPINAL ROD AND SPINAL HOOKS | Buckman Co., Inc. | 1989-04-26 | 204 | 0 |
| K884740 | EURO-MED LIGHT TOUCH BIOPSY PUNCH | Buckman Co., Inc. | 1989-03-06 | 112 | 0 |
| K884868 | OBSTETRICAL SAFETY SYSTEM | Buckman Co., Inc. | 1989-03-01 | 100 | 0 |
| K882322 | CONTINUUM KNEE SYSTEM (CKS) | Buckman Co., Inc. | 1989-02-08 | 247 | 0 |
| K881841 | DANNINGER TRIMCHECK(TM) PORTABLE & DESK TOP MODELS | Buckman Co., Inc. | 1988-12-13 | 225 | 0 |
| K882605 | EURO-MED CLEAR-VUE DISPOSABLE VAGINAL SPECULUM | Buckman Co., Inc. | 1988-09-15 | 83 | 0 |
| K882831 | ACE CANCELLOUS BONE SCREW | Buckman Co., Inc. | 1988-08-01 | 24 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda