Atlas FDA

Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

POV — Predicate Candidate Screening

28 FDA 510(k) clearances under this product code; the 50 most recent screened below.

148 daysmedian FDA review time
296 days90th percentile
28clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K252228Seaman Pro/SeamanCheckcells, Inc.2026-04-092670
K242830LensHooke X3 PRO Semen Quality Analyzer; LensHooke X3 PRO SEBonraybio Co., Ltd.2025-05-302530
K242388LensHooke X12 PRO Semen Analysis SystemBonraybio Co., Ltd.2025-05-092700
K243114SQA-iOw Sperm Quality AnalyzerMedical Electronic Systems , Ltd.2025-05-022140
K241628YO Home Sperm TestMedical Electronic Systems , Ltd.2024-11-291760
K220828SQA-iO Sperm Quality AnalyzerMedical Electronic Systems , Ltd.2023-08-075030
K202089LensHooke X1 PRO Semen Quality Analyzer, LensHooke X1 PRO SEBonraybio Co., Ltd.2020-10-28920
K183602SwimCount Sperm Quality TestMotilitycount Aps2019-06-271830
K180343LensHooke X1 Pro Semen Quality Analyzer, LensHooke X1 Semen Bonraybio Co., Ltd.2018-11-162820
K172514Trak Plus Male Fertility Testing SystemSandstone Diagnostics, Inc.2017-11-17880
K161493YO Home Sperm TestMedical Electronic Systems , Ltd.2016-11-081600
K153683Trak Male Fertility Testing SystemSandstone Diagnostics, Inc.2016-05-161460
K100341SPERMCHECK FERTILITYPrinceton BioMeditech Corp.2010-05-04880
K073039SPERMCHECK VASECTOMYPrinceton BioMeditech Corp.2008-01-24870
K071737GENERAL SEMEN ANALYSIS KITDyn-Bioshaf (2006) , Ltd.2007-10-251210
K063864QWIKCHECK TEST STRIPS- REAGENT STRIPS FOR SEMEN ANALYSISMedical Electronic Systems , Ltd.2007-03-26870
K041039FERTELL MALE FERTILITY TESTGenosis , Ltd.2004-07-20890
K032874HBA SPERM-HYALURONAN BINDING ASSAYBiocoat, Inc.2003-11-24700
K024337GENERAL SEMEN ANALYSIS (GSA) KITBioshaf , Ltd.2003-07-031880
K021746SQA V, SPERM QUALITY ANALYZERMedical Electronic Systems, LLC2002-09-201150
K012805AUTOMARQERHamilton Thorne Research2002-03-132040
K012352SQA, SPERM QUALITY ANALYZERMedical Electronic Systems, LLC2001-09-21580
K011679FERTILMARQ HOME DIAGNOSTIC SCREENING TEST KIT FOR MALE INFEREmbryotech Laboratories, Inc.2001-08-15770
K990184AUTOMARQERHamilton Thorne Research1999-03-19580
K983473FERTILMARQ TEST KITEmbryotech Laboratories, Inc.1998-12-17760
K915229SEMEN ANALYSIS KITHumagen Fertility Diagnostics, Inc.1994-08-3010140
K894949SQAUnited Medical Systems, Inc.1989-12-291480
K881765CTS-3060 AUTOMATED SEMEN ANALYZERMotion Analysis Corp.1989-02-152960

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