Atlas FDA

Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Ansell Healthcare Products, Inc. · Predicate Candidate Screening

10 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

51 daysmedian FDA review time
133 days90th percentile
10clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K111139DERMA PRENE ISOTOUCH GREEN STERILE POWDER-FREE POLYISOPRENE Ansell Healthcare Products, Inc.2011-09-021332
K082457MICRO-TOUCH NITRATEX STERILE NITRILE POWDER-FREE BLUE EXAMINAnsell Healthcare Products, Inc.2008-11-10760
K042817MICRO-TOUCH SMOOTH NITRILE POWDER-FREE BLUE EXAMINATION GLOVAnsell Healthcare Products, Inc.2004-12-06550
K023153MICRO-TOUCH NEXT STEP POWDER FREE MEDICAL EXAMINATION GLOVESAnsell Healthcare Products, Inc.2002-11-13510
K013603MODIFICATION TO:MICRO TOUCH (R) POWDER FREE LATEX SURGICAL GAnsell Healthcare Products, Inc.2001-11-13130
K013604MODIFICATION TO: ULTRALON (R) POWDER FREE LATEX SURGICAL GLOAnsell Healthcare Products, Inc.2001-11-13130
K011593MICRO-TOUCH NITRILE POWDER FREE SYNTHETIC MEDICAL EXAMINATIOAnsell Healthcare Products, Inc.2001-06-21280
K010961X-TENDA CUFF POWDER FREE NON-STERILE LATEX EXAMINATION GLOVEAnsell Healthcare Products, Inc.2001-05-31620
K003771ENCORE POWDER-FREE LATEX SURGICAL GLOVES, ORTHOPAEDIC WITH PAnsell Healthcare Products, Inc.2001-01-16410
K003769ENCORE MICROPTIC POWDER FREE LATEX SURGICAL GLOVES, MODEL 87Ansell Healthcare Products, Inc.2000-12-22160

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