Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

FRA — Predicate Candidate Screening

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

190 daysmedian FDA review time
399 days90th percentile
36clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K252128Zener® (model ZEN-001-B1)Uvx, Inc.2025-09-15700
K241140ViroZap Indoor Air Purifier, In Duct Model 1008Applied Photonix, LLC2024-08-01990
K232642AirKEE T900Healkee Medical Pte, Ltd.2024-05-232670
K232933AirKEE P900Healkee Medical Pte, Ltd.2024-05-162390
K232645Airgle Room Air PurifierAirgle Corporation2024-02-161700
K221540Synexis Sphere RxSynexis, LLC2023-06-143830
K222702RGS; RGS MiniGenesis Air, Inc.2023-06-022680
K223328PurgoAeroclean Technologies, Inc.2022-11-30300
K213753PurgoAeroclean Technologies, LLC2022-06-011830
K212644Aura StormInvictus Lighting2022-05-262790
K212824Bluezone Model RX-450 Air PurifierBluezone Products, Inc.2022-02-171670
K211139CUBE Air PurifierSamsung Electronics Co., Ltd.2021-11-262240
K211194Molekule Air ProMolekule, Inc.2021-08-201210
K202766EOS Air CleanerGuangzhou Ajax Medical Equipment Co., Ltd.2021-06-112630
K202339Molekule Air Mini, Molekule Air Mini +Molekule, Inc.2021-02-231900
K203189AEROCURE-MDAerobiotix, Inc.2021-01-21860
K201220Aerus Medical Guardian,model F170AAerus Medical, LLC2020-06-17420
K200500Molekule Air Pro RXMolekule, Inc.2020-04-15470
K161468Transformair Indoor Air PurifierTransformair, LLC2017-02-082570
K133800ODOROX(R) IDU/RX (TM) IN-DUCT MODELS, ODOROX(R) IDU/RX (TM) Hgi Industires2014-12-193710
K062716ECO-RX AIR PURIFIER WITH UV LIGHT, MODEL RX-400Eco-Rx, Inc.2006-10-27450
K052732ABRACAIR AIR CLEANER, MODEL QTZ300-60; ABRACAIR AIR CLEANER,Abracair, Inc.2006-02-241480
K033448ELECTRO-OPTICAL AIR STERILIZER WITH IONIZERJohn Mfg., Ltd.2004-07-122570
K023830AIROCIDE TI02Kes Science & Technology, Inc.2003-02-04780
K980745SECOND WIND AIR PURIFIERMonagan Ent., Inc.1999-04-024000
K972064MICROCON 800MUV, MICROCON 400MUV, MICROCON EXC-BUVBiological Controls, Inc.1997-12-011810
K954448VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEMSchiff & Co.1996-10-283990
K960833VIOTEC S-4000-CR SECURITY SERIES ULTRAVIOLET GERMICIDAL AIR Uv Technologies, Inc.1996-07-251470
K951981RXAIR 3000Clean Air Research & Development1995-10-121680
K943521VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURESchiff & Co.1995-02-142090
K933454DYNAMIC GERMICIDAL AIR PURIFICATION SYSTEML&H Airco1994-09-164290
K932803CLESTRACLEAN(R) ROOM AIR PURIFIERClestra Cleanroom Technology, Inc.1994-05-123370
K934914ICS 9400 ULTRAVIOLET AIR PURIFIERMedair, Inc.1994-04-131820
K920965STRAIGHT-LINES I.V. ORGANIZERTaylor Bio-Medical, Inc.1993-04-074010
K884579UV AIR STERILIGHTAllseasons Environmental Control, Inc.1988-12-12390
K860132AIR CARE AIR SANITIZERCooper-Hewitt Electric Co.1987-01-133640

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