Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Alliance Medical Corp. · Predicate Candidate Screening
36 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
90 daysmedian FDA review time
315 days90th percentile
36clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K060648 | REPROCESSED PHACOEMULSIFICATION TIPS | Alliance Medical Corp. | 2007-03-19 | 371 | 0 |
| K061045 | REPROCESSED ELECTROPHYSIOLOGY CATHETERS | Alliance Medical Corp. | 2006-08-31 | 139 | 0 |
| K060049 | REPROCESSED COMPRESSION SLEEVES | Alliance Medical Corp. | 2006-02-24 | 49 | 0 |
| K060091 | ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES | Alliance Medical Corp. | 2006-02-17 | 36 | 0 |
| K053316 | REPROCESSED COMPRESSION SLEEVES | Alliance Medical Corp. | 2006-02-13 | 76 | 0 |
| K052918 | REPROCESSED EXTERNAL FIXATION DEVICES | Alliance Medical Corp. | 2006-01-27 | 102 | 0 |
| K052414 | REPROCESSED ELECTROPHYSIOLOGY CATHETER | Alliance Medical Corp. | 2005-11-16 | 75 | 0 |
| K052603 | REPROCESSED DAIG LIVEWIRE ELECTROPHYSIOLOGY CATHETERS | Alliance Medical Corp. | 2005-11-16 | 56 | 26 |
| K052062 | ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION D | Alliance Medical Corp. | 2005-08-25 | 27 | 0 |
| K052064 | ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION D | Alliance Medical Corp. | 2005-08-25 | 27 | 0 |
| K052065 | ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION D | Alliance Medical Corp. | 2005-08-22 | 24 | 0 |
| K051554 | ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION D | Alliance Medical Corp. | 2005-06-29 | 16 | 0 |
| K043358 | REPROCESSED ULTRASONIC SCALPELS | Alliance Medical Corp. | 2005-06-06 | 182 | 0 |
| K043392 | REPROCESSED ELECTROPHYSIOLOGY CATHETERS | Alliance Medical Corp. | 2005-03-25 | 105 | 0 |
| K043393 | REPROCESSED EP TECHNOLOGIES ELECTROPHYSIOLOGY CATHETERS | Alliance Medical Corp. | 2005-03-23 | 103 | 0 |
| K033436 | REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER | Alliance Medical Corp. | 2005-03-16 | 505 | 0 |
| K041978 | REPROCESSED DIAMOND BURS | Alliance Medical Corp. | 2004-11-23 | 123 | 0 |
| K030279 | REPROCESSED ELECTROPHYSIOLOGY CATHETER | Alliance Medical Corp. | 2003-10-03 | 249 | 0 |
| K030109 | ELECTROPHYSIOLOGY CATHETER | Alliance Medical Corp. | 2003-08-08 | 207 | 1 |
| K032058 | MODIFICATION TO REPROCESSED SYNTHES EXTERNAL FIXATION DEVICE | Alliance Medical Corp. | 2003-07-30 | 28 | 0 |
| K030026 | REPROCESSED ELECTROPHYSIOLOGY CATHETER | Alliance Medical Corp. | 2003-05-02 | 119 | 0 |
| K024087 | REPROCESSED COMPRESSION SLEEVES | Alliance Medical Corp. | 2003-03-11 | 90 | 0 |
| K024074 | REPROCESSED COMPRESSION SLEEVES | Alliance Medical Corp. | 2003-03-07 | 87 | 0 |
| K024015 | REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS | Alliance Medical Corp. | 2003-03-04 | 90 | 0 |
| K023714 | REPROCESSED EXTERNAL FIXATION DEVICE | Alliance Medical Corp. | 2003-02-03 | 90 | 0 |
| K012708 | ELECTROPHYSIOLOGY CATHETER | Alliance Medical Corp. | 2002-08-13 | 364 | 27 |
| K012623 | REPROCESSED EXTERNAL FIXATION DEVICE | Alliance Medical Corp. | 2002-06-24 | 315 | 0 |
| K012645 | REPROCESSED EBI EXTERNAL FIXATION DEVICES | Alliance Medical Corp. | 2002-06-24 | 315 | 0 |
| K012648 | REPROCESSED HOWMEDICA EXTERNAL FIXATION DEVICES | Alliance Medical Corp. | 2002-06-24 | 315 | 0 |
| K012631 | REPROCESSED SOFT TISSUE ABLATORS | Alliance Medical Corp. | 2001-12-06 | 115 | 0 |
| K011192 | COMPRESSIBLE LIMB SLEEVE | Alliance Medical Corp. | 2001-11-26 | 221 | 0 |
| K012652 | REPROCESSED DYONICS ARTHROSCOPIC BURS | Alliance Medical Corp. | 2001-11-08 | 87 | 7 |
| K012605 | REPROCESSED ATHROSCOPICS BURS | Alliance Medical Corp. | 2001-11-07 | 86 | 8 |
| K012635 | REPROCESSED STRYKER ARTHROSCOPIC SHAVERS | Alliance Medical Corp. | 2001-11-07 | 86 | 8 |
| K012603 | REPROCESSED AUTOSUTURE UNIPOLAR LAPAROSCOPIC/ENDOSCOPIC INST | Alliance Medical Corp. | 2001-11-07 | 86 | 0 |
| K012625 | REPROCESSED UNIPOLAR LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTS | Alliance Medical Corp. | 2001-10-22 | 70 | 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