Atlas FDA

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

KZE — Predicate Candidate Screening

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

89 daysmedian FDA review time
288 days90th percentile
53clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K121270BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEMBioject Medical Technologies, Inc.2012-07-19840
K111517PHARMAJET STRATIS 0.5 ML NEEDLE-FREE INJECTION SYSTEM MODEL Pharmajet, Inc.2011-07-27550
K110456PHARMAJET 0.1 ML INTRADERMAL NEEDLE-FREE INJECTION SYSTEMPharmajet, Inc.2011-03-02140
K090959LECTRAJET NEEDLE-FREE INJECTION SYSTEM, MODEL: M3 RAD'Antonio Consultants International, Inc. (Dci)2009-12-242620
K090003ZETAJETBioject, Inc.2009-04-02901
K081532PHARMAJET NEEDLE-FREE INJECTION SYSTEMPharmajet, Inc.2009-02-262690
K082138AIRGENT, MODEL AG7000010Perfaction, Inc.2009-01-231780
K060819COOL.CLICK 2Medical House Products Limited2006-06-16810
K051985BIOVALVE MINI-JECT NEEDLEFREE INJECTORBiovalve Technologies, Inc.2005-08-17260
K050734COOL.CLICKBioject, Inc.2005-06-03740
K041239GENESIS MEDICAL TECHNOLOGIES, INC. PHARMAJET NEEDLE-FREE INJGenesis Medical Technology, Inc.2004-11-081810
K041280HUMAN SUBCUTANEOUS INJECTOR, MODEL HSI 500Felton International, Inc.2004-06-24420
K032976BIOVALVE MINIJECT NEEDLE-FREE INJECTION SYSTEM, MODEL FG-01-Biovalve Technologies, Inc.2004-04-162050
K024018AVANT GUARDIAN 101Avant Medical Corporation2003-01-17440
K020786INJEX NEEDLE-FREE INJECTION SYSTEM; ROJEX NEEDLE-FREE INJECTRosch AG Medizintechnic2002-09-251980
K022502INJEX 30 NEEDLE FREE INJECTION SYSTEM, MODEL 100000Equidyne Systems, Inc.2002-09-05380
K022148INJEX 30 NEEDLE FREE INJECTION SYSTEMEquidyne Systems, Inc.2002-07-23210
K013256BI-3M NEEDLE-FREE INJECTOR SYSTEMFelton International, Inc.2001-12-07670
K003741JET SYRINGE MODEL-100500Equidyne Systems, Inc.2001-06-011790
K003908SEROJETBioject, Inc.2001-03-08790
K003864INJEX 50 SYSTEMEquidyne Systems, Inc.2001-03-06830
K994384CLICKERBioject, Inc.2000-06-221770
K991294MODIFICATION TO MEDI-JECT CORPORATION MEDI-JECTOR CHOICE NEEMedi-Ject Corp.1999-04-2380
K980082J-TIP NEEDLESS INJECTORNational Medical Products, Inc.1998-03-04540
K973254J-TIP INJECTORNational Medical Products, Inc.1997-11-24870
K960373BIOJECTOR 2000 MODEL 1B02000Bioject, Inc.1997-03-054040
K962625VITAJETVitajet Corp.1996-12-101580
K962956MEDI-JECTOR CHOICE NEEDLE-FREE INSULIN DELIVERY SYSTEMMedi-Ject Corp.1996-10-07690
K960285MEDI-JECT CORPORATION MEDI-JECTOR NEEDLE-FREE BIO-TROPIN DDRMedi-Ject Corp.1996-04-17890
K945548MEDIVAXVitajet Corp.1995-11-203710
K945873HYPEX(TM) JET INJECTOREquidyne Systems, Inc.1995-08-182600
K920631BIOJECT JET INJECTION SYSTEMBioject, Inc.1994-06-288670
K921797PRECI-JET 50Hmi Industries, Inc.1992-11-172170
K923326OPHTHALMIC VISCOINJECTOR DRIVESynergetics, Inc.1992-09-30850
K913018MED-E-JET INJECTORMed-E-Jet D1991-09-16690
K905062INJECTOR, INSULINSound 2000 Medical Systems, Inc.1991-03-151260
K893215VITAJET(INSULIN JET INJECTION DEVICE)Vitajet Industriae Comercioltda.1990-05-073750
K884293J-TIP INJECTOR SYSTEMCalifornia Medical Innovations, Inc.1989-01-09890
K883847DERATA MEDI-JECTOR VDerata Corp.1988-10-31490
K864984ROBINJECTInternational Medical Products, Inc.1987-06-291890
K861687BIOJECTOR SYRINGE SYSTEMBioject, Inc.1987-04-233560
K864561DERATA MEDI-JECTOR IVDerata Corp.1987-02-19920
K861582INJET-100, FLUID INJECTORInjet Medical Products, Inc.1987-02-032800
K853031JECT-AIDAutoject Systems, Inc.1986-01-011670
K850754MEDAJET XL - JET INJECTORMada Medical Products, Inc.1985-12-102880
K844244DERATA MEDI-JECTOR PRODerata Corp.1985-07-052460
K851809VACUUM COMPRESSION INJECTORUci Corp.1985-07-01660
K851181PRECI-JET 50Ulster Scientific, Inc.1985-06-06730
K851029NEW VITAJETAndrew V. Stadler1985-05-23720
K844111DERATA MEDI-JECTOR IIIDerata Corp.1984-11-28360

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