Atlas FDA

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

EMX — Predicate Candidate Screening

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

65 daysmedian FDA review time
283 days90th percentile
47clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K220326PosiSep X BAM Hemostat Dressing/Intranasal SplintHemostasis, LLC2022-11-142830
K041446NASALCEASELes Laboratorires Brothier, S.A.2004-07-01300
K000108RAPID RHINO-ANTERIOR 90MM, MODEL RR-A 90, RAPID RHINO-POSTERBhk Holding2000-05-231300
K993362HYLASINEBiomatrix, Inc.2000-03-131590
K983276HYDROFERA BACTERISTATIC NASAL DRESSINGHydrofera, LLC1999-09-143620
K982731MEROGEL NASAL DRESSING AND SINUS STENTXomed, Inc.1999-02-021810
K984069ENTAXIS NASAL PACKINGLes Laboratorires Brothier, S.A.1999-01-25700
K981966NOSEBLEED NOSECLIPMichael M. Knott, M.D.1998-08-14710
K973656DISPOSABLE SILICONE EPISTAXIS CATHETERSpecialty Surgical Products, Inc.1997-11-18540
K973085ULTRACELL PACKING WITH SLEEVEUltracell Medical Technologies, Inc.1997-11-18920
K972922VYKER SILICONE EPISTAXIS CATHETER V-27030, VYKER SILICONE EPInterview Medical Technology Corp.1997-10-08610
K972459RHINOCELL NASAL PACKINGSBoston Medical Products, Inc.1997-08-04340
K972078POST-STOP EPISTAXIS CATHETERBoston Medical Products, Inc.1997-07-10370
K972076EPI-MAX EPISTAXIS CATHETERBoston Medical Products, Inc.1997-06-26230
K972077EPI-STOP EPISTAXIS CATHETERBoston Medical Products, Inc.1997-06-26230
K971411DISPOSABLE SILICONE EPISTAXIS CATHETER V-27030/DISPOSABLE SIBentec Medical, Inc.1997-06-03480
K971000EPISTAXIS NASAL PACKInvotec International, Inc.1997-05-14560
K964113IVALON NASAL PACKING W/DRAWSTRING (8.0CM & 4.5CM), IVALON NAM-Pact Worldwide Management Corp.1996-11-07230
K963856RAND NASAL PACKINGRand Scientific Corp.1996-10-18230
K962133EXPANDACELL INJECTO-PAKShippert Medical Technologies Corp.1996-08-01590
K960228EXPANDACELL INJECTO-PAK NASAL PACKShippert Medical Technologies Corp.1996-02-27410
K955593EXPANDACELL ANATOMICAL POSTERIOR NASAL PACK W/& WITHOUT AIRWShippert Medical Technologies Corp.1995-12-22150
K954845EXPANDACELL INJECTO-PAK NASAL PACKShippert Medical Technologies Corp.1995-11-27350
K954491HYDROCELL NASAL AND SINUS PACKSSmith & Nephew Richards, Inc.1995-11-15490
K945554EPISTAXIS BALLOON CATHETER WITH PACKINGUltracell Medical Technologies, Inc.1995-02-17950
K950024EXPANDACELL NASAL PACK WITH AIRWAYShippert Medical Technologies Corp.1995-02-17440
K945556ANTERIOR/POSTERIOR EPISTAXIS CATHETERUltracell Medical Technologies, Inc.1995-01-18650
K943718EPISTAT-II NASAL CATHETERMerocel Corp.1994-09-16460
K933800FLUOROFILM(R)American Custom Medical, Inc.1994-06-243240
K935724THE EXPANDACELL SINUS PACKDenver Splint Co.1994-05-121620
K924944INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRAWestmed Intl.1993-07-022750
K920394MEROCEL EPISTACIS KITMerocel Corp.1993-03-184130
K924542NASAL-SINUS PACKINGUltracell Medical Technologies, Inc.1993-02-121570
K920358ULTRACELL NASAL PACKINGUltracell Medical Technologies, Inc.1992-11-303083
K921199EPISTAXIS NASAL BALLOON CATHETERSmith & Nephew Richards, Inc.1992-07-081180
K912524EXPANDACEL NASAL TAMPONS, MODIFICATIONSurgitrend, Ltd.1991-08-15730
K904624EXPANDACEL NASAL TAMPONSRon Shippert, MD1991-03-211610
K900583MODIFIED BIVONA EPISTAXIS CATHETERBivona Medical Technologies1990-08-091830
K900171EXPANDACEL NASAL TAMPONSSurgitrend, Ltd.1990-06-141530
K901310ULTRASTAT NASAL CATHETERInvotec International, Inc.1990-06-14860
K896248INNOVATIONS NASAL TAMPONInnovations by Necessity, Inc.1990-04-131650
K841040FOX POST NASAL BALLOON CATHETERInmed Corp.1984-08-171580
K821584EPISTAXIS CATHETER/KITBivona Medical Technologies1982-06-14130
K811496GOTTSCHALK NASOSTAT SLIM LINE, ADULT/SM.Narco Scientific1981-06-16200
K800175NASOSTATEdward Weck, Inc.1980-02-21240
K781615NASOSTATNasostat, Inc.1978-10-11200
K781631ECHO-OILEcho Laboratories, Inc.1978-10-10150

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