Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
U.S. Medical Products, Inc. · Predicate Candidate Screening
24 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
106 daysmedian FDA review time
303 days90th percentile
24clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K962215 | CONSENSUS POSTERIOR STABILIZED KNEE-INTERCONDYLAR NOTCH ROUT | U.S. Medical Products, Inc. | 1996-08-15 | 66 | 0 |
| K954818 | CONSENSUS POSTERIOR STABILIZED KNEE | U.S. Medical Products, Inc. | 1996-05-22 | 215 | 0 |
| K953443 | CONSENSUS PCL SUBSITUTING TIBIAL INSERT | U.S. Medical Products, Inc. | 1996-04-26 | 284 | 0 |
| K952943 | CONSENSUS ALL POLY TIBIA | U.S. Medical Products, Inc. | 1996-04-01 | 280 | 0 |
| K960302 | CONSENSUS ACETABULAR SHELL, ALL UHMWPE | U.S. Medical Products, Inc. | 1996-04-01 | 70 | 0 |
| K960340 | CONSENSUS APEX DOME HOLE PLUG | U.S. Medical Products, Inc. | 1996-03-15 | 51 | 0 |
| K960151 | CONSENSUS 26MM COCRMO FEMORAL HEAD | U.S. Medical Products, Inc. | 1996-02-21 | 41 | 0 |
| K960156 | CONSENSUS 32MM COCRMO FEMORAL HEAD | U.S. Medical Products, Inc. | 1996-02-21 | 41 | 0 |
| K960339 | CONSENSUS 22MM COCRMO FEMORAL HEAD | U.S. Medical Products, Inc. | 1996-02-21 | 28 | 0 |
| K955386 | CONSENSUS ZIRCONIA FEMORAL HEAD | U.S. Medical Products, Inc. | 1996-02-20 | 90 | 0 |
| K953792 | CONSENSUS ZIRCONIA HEAD SIZE -3.5, 0, +5 | U.S. Medical Products, Inc. | 1995-11-06 | 84 | 0 |
| K945589 | CONSENSUS(TM) KNEE COBALT CHROME NONPOROUS STEMMED TIBIAL BA | U.S. Medical Products, Inc. | 1995-05-31 | 198 | 0 |
| K950013 | CONSENSUS(TM) ORTHOPEDIC DRILL BIT | U.S. Medical Products, Inc. | 1995-05-05 | 122 | 0 |
| K946197 | CONSENSUS(TM) PATELLA REAMER | U.S. Medical Products, Inc. | 1995-04-05 | 106 | 0 |
| K944946 | CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER | U.S. Medical Products, Inc. | 1995-02-01 | 117 | 0 |
| K945186 | CONSENUS HIP SYSTEM -- ACETABULAR REAMER | U.S. Medical Products, Inc. | 1995-01-27 | 95 | 0 |
| K945189 | CONSENSUS HIP SYSTEM -- CALCAR PLANER | U.S. Medical Products, Inc. | 1995-01-27 | 95 | 0 |
| K945208 | CONSENSUS HIP SYSTEM -- TROCHANTERIC CUTTER | U.S. Medical Products, Inc. | 1995-01-27 | 94 | 0 |
| K932837 | CONSENSUS KNEE SYSTEM - PRIMARY KNEE | U.S. Medical Products, Inc. | 1994-09-27 | 473 | 0 |
| K935193 | CONSENSUS HIP SYSTEM- POROUS COATED TITIANIUM FEMORAL STEM | U.S. Medical Products, Inc. | 1994-08-18 | 296 | 0 |
| K935453 | CONSENSUS(TM) HIP SYSTEM-HA COATED TIANIUM FEM STEM | U.S. Medical Products, Inc. | 1994-07-13 | 243 | 0 |
| K933499 | CONSENSUS HIP SYSTEM- NON-POROUS TITANIUM FEMORAL STEM | U.S. Medical Products, Inc. | 1994-05-18 | 303 | 0 |
| K922561 | CONSENSUS(TM) TOTAL HIP SYSTEM | U.S. Medical Products, Inc. | 1993-07-21 | 413 | 0 |
| K922560 | CONSENSUS(TM) BIPOLAR SYSTEM | U.S. Medical Products, Inc. | 1992-09-11 | 105 | 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