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7,525 catalysts · 3,350 8k filing · 1,096 grant · 1,000 device adverse event · 580 earnings · 550 approval · 430 device 510k

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  • 8k filing3,350
  • grant1,096
  • device adverse event1,000
  • earnings580
  • approval550
  • device 510k430
device pma
248
  • phase 2 completion172
  • drug shortage133
  • recall121
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Mar 9, 2026

    50
    ›Mar 11, 2026grant158d agoLSU PENNINGTON BIOMEDICAL RESEARCH CTR — Breath Biomarkers of Disease and Health Outcomes (BREATHE OUT)

    GM grant. $225,000. PI: Jacob T Mey

    full page →nih reporter ↗
    ›Mar 12, 2026approval157d agoCOSENTYX (SECUKINUMAB) — FDA approvalNOVARTIS AG

    Sponsor: NOVARTIS PHARMS CORP. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Mar 12, 2026approval157d agoCOSENTYX (SECUKINUMAB) — FDA approvalNOVARTIS AG

    Sponsor: NOVARTIS PHARMS CORP. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Mar 12, 2026approval157d agoPROMETHAZINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN HYDROBROMIDE) — FDA approvalPROMETHAZINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE

    Sponsor: HETERO LABS LTD III. Form: SYRUP. Route: ORAL

    full page →PROMETHAZINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE →fda approvals ↗
    ›Mar 12, 2026approval157d agoTRULICITY (DULAGLUTIDE) — FDA approvaldulaglutide

    Sponsor: ELI LILLY AND CO. Form: INJECTABLE. Route: INJECTION

    full page →dulaglutide →fda approvals ↗
    ›Mar 12, 2026approval157d agoSOLIQUA 100/33 (INSULIN GLARGINE) — FDA approvalToujeo LA

    Sponsor: SANOFI-AVENTIS US. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →Toujeo LA →fda approvals ↗
    ›Mar 12, 2026approval157d agoPOTASSIUM PHOSPHATES (POTASSIUM PHOSPHATE, DIBASIC) — FDA approvalHospira Inc

    Sponsor: CAPLIN. Form: SOLUTION. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Mar 12, 2026approval157d agoFINGOLIMOD HYDROCHLORIDE — FDA approvalFINGOLIMOD HYDROCHLORIDE

    Sponsor: BIOCON LTD. Form: CAPSULE. Route: ORAL

    full page →FINGOLIMOD HYDROCHLORIDE →fda approvals ↗
    ›Mar 12, 2026approval157d agoFINGOLIMOD HYDROCHLORIDE — FDA approvalFINGOLIMOD HYDROCHLORIDE

    Sponsor: BIOCON LTD. Form: CAPSULE. Route: ORAL

    full page →FINGOLIMOD HYDROCHLORIDE →fda approvals ↗
    ›Mar 12, 2026approval157d agoADLYXIN (LIXISENATIDE) — FDA approvalADLYXIN

    Sponsor: SANOFI-AVENTIS US. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →ADLYXIN →fda approvals ↗
    ›Mar 12, 2026approval157d agoSUNLENCA (LENACAPAVIR SODIUM) — FDA approvallenacapavir sodium LA

    Sponsor: GILEAD SCIENCES INC. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →lenacapavir sodium LA →fda approvals ↗
    ›Mar 12, 2026approval157d agoSUNLENCA (LENACAPAVIR SODIUM) — FDA approvallenacapavir sodium LA

    Sponsor: GILEAD SCIENCES INC. Form: TABLET. Route: ORAL

    full page →lenacapavir sodium LA →fda approvals ↗
    ›Mar 12, 2026approval157d agoPOMALIDOMIDE — FDA approvalTeva Pharmaceuticals USA Inc

    Sponsor: TEVA PHARMS USA. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Mar 12, 2026device 510k157d agoHsiner Co., Ltd. — VPAP Pediatric Face Mask (510k cleared)

    Product code: CBK. Advisory committee: Anesthesiology. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoInvera Medical — InVera Infusion Device (510k cleared)

    Product code: KRA. Advisory committee: Cardiovascular. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoBionit Labs Srl — Remote Wave Electrode (AE03-50); Remote Wave Electrode (AE03-60) (510k cleared)

    Product code: GXY. Advisory committee: Neurology. Type: Special

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoFree Flow Medical, Inc. — LungFlow Basket Catheter (510k cleared)

    Product code: KTI. Advisory committee: Ear, Nose, Throat. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoGuangzhou Ajax Medical Equipment Co., Ltd. — Dental X-RAY Unit (AJX200) (510k cleared)

    Product code: EHD. Advisory committee: Dental. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoHR Healthcare — Liv Pre-lubricated Intermittent Catheter (510k cleared)HCA Healthcare, Inc.

    Product code: EZD. Advisory committee: Gastroenterology, Urology. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoA Cute Baby, Inc. — Mini Moon electric breast pump (PA221); Moon Wave electric breast pump (PA220) (510k cleared)

    Product code: HGX. Advisory committee: Obstetrics/Gynecology. Type: Abbreviated

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoDigestaid - Artificial Intelligence Development SA — Deep Capsule® (Deep Capsule US) (510k cleared)

    Product code: QZF. Advisory committee: Gastroenterology, Urology. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoProdeon Medical, Inc. — Urocross Expander System (Model Numbers ES2018 and ES3025) (510k cleared)

    Product code: QKA. Advisory committee: Gastroenterology, Urology. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoStryker Leibinger GmbH & Co KG — MEDPOR Customized Implant Kit (510k cleared)

    Product code: FWP. Advisory committee: General, Plastic Surgery. Type: Special

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoAIRICU, Inc. — Medical Mesh Nebulizer (AirICU Max+) (510k cleared)

    Product code: SFP. Advisory committee: Anesthesiology. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoSpectrum Medical S.R.L. — Quantum PureFlow Standard Heat Exchanger Medium Flow 1/4 W (510k cleared)

    Product code: DTR. Advisory committee: Cardiovascular. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoNanjing Mijo Technology Co., Ltd. — Power Mobility Scooter (MJMA01, MJMA02) (510k cleared)Nanjing Miracle Biotechnology Co Ltd

    Product code: INI. Advisory committee: Physical Medicine. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoSpectrum Medical S.R.L. — Quantum Perfusion Blood Oxygenator ECC VT160-E3 (VT160-E3); Quantum Perfusion Blood Oxygenator ECC VT200-E3 (VT200-E3); Quantum Perfusion Blood Oxygenator VT75- E3 (VT75- E3); (510k cleared)

    Product code: DTZ. Advisory committee: Cardiovascular. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoTermosalud S.L. — Zionic Pro Max (EMS) (510k cleared)

    Product code: NGX. Advisory committee: Physical Medicine. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoZimmer, Inc. — Affixus Retrograde Femoral Nailing System (510k cleared)

    Product code: HSB. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoMaterialise NV — Mimics Thoracic Planner (510k cleared)MATERIALISE NV

    Product code: LLZ. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoGenadyne Biotechnologies, Inc. — Genadyne ASTRA NPWT (510k cleared)POP Biotechnologies Inc

    Product code: OMP. Advisory committee: General, Plastic Surgery. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoSignature Orthopaedics Pty, Ltd. — Evolve AP Cup, World Finned Cup, World G-Zero Liner and Oddball Femoral Head (510k cleared)

    Advisory committee: Unknown. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoMedtronic Minimed, Inc. — MiniMed Flex pump (510k cleared)Medtronic USA Inc

    Product code: QFG. Advisory committee: Clinical Chemistry. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoTyto Care , Ltd. — Tyto Stethoscope (G3) (510k cleared)

    Product code: DQD. Advisory committee: Cardiovascular. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoTrax Surgical, Inc. — Trax EX Anchor (510k cleared)

    Product code: MBI. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoAllevion Medical, LLC — VantageTM Lumbar Decompression Kit (510k cleared)

    Product code: HRX. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoTaurus Endoscopy — Taurus Clip (510k cleared)

    Product code: PKL. Advisory committee: Gastroenterology, Urology. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoImplantcast GmbH — implaFit® short stems (510k cleared)

    Product code: LZO. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device 510k157d agoRapid Medical , Ltd. — Tigertriever 25 Revascularization Device (510k cleared)

    Product code: NRY. Advisory committee: Cardiovascular. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 12, 2026device pma157d agoAbbott Molecular, Inc. — Alinity m HR HPV (PMA supplement)

    Supplement type: Real-Time Process. Product code: MAQ. Advisory committee: MI. Decision: APPR

    full page →fda device pma ↗
    ›Mar 12, 2026device pma157d agoBoston Scientific Corporation — Ranger Paclitaxel-Coated PTA Balloon Catheter (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: ONU. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Mar 12, 2026device pma157d agoEuclid Vision Corporation — Euclid Orthokeratology (oprifocon A) Contact Lenses for Overnight Wear and Euclid Orthokeratology (tisilfocon A) Contact (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: NUU. Advisory committee: OP. Decision: APPR

    full page →fda device pma ↗
    ›Mar 12, 2026device pma157d agoIntegrum AB — OPRA Implant System (PMA supplement)

    Supplement type: Normal 180 Day Track No User Fee. Product code: PJY. Advisory committee: OR. Decision: APPR

    full page →fda device pma ↗
    ›Mar 12, 2026device pma157d agoQ-Med AB — RESTYLANE INJECTABLE GEL (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LMH. Advisory committee: SU. Decision: OK30

    full page →fda device pma ↗
    ›Mar 12, 2026device pma157d agoNeomend, Inc. — TRIDYNE™ Vascular Sealant (PMA supplement)

    Supplement type: 30-Day Notice. Product code: NBE. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Mar 12, 2026device pma157d agoNeomend, Inc. — PROGEL™ Pleural Air Leak Sealant (PMA supplement)

    Supplement type: 30-Day Notice. Product code: NBE. Advisory committee: AN. Decision: OK30

    full page →fda device pma ↗
    ›Mar 12, 2026device recall157d agoBrahms GmbH device recall (Cls II)

    B.R.A.H.M.S PlGF Plus KRYPTOR, Catalog Number: 859075N. in vitro diagnostic test for Placental Growth Factor — Reason: Customers have observed quality control values out of range at the lowest quality control level (QC Level 1) for the PIGF assay which require troubleshooting steps to resolve. If Quality Controls are not performed according to the Instructions for Use, the underestimation of QC1 may go undetected and could contribute to falsely elevated sFlt-1/PlGF ratio results. A falsely elevated sFlt-1/PlGF ratio may result in a higher-risk classification for progression to preeclampsia with severe features potentially leading to intensified clinical monitoring. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 12, 2026device recall157d agoStryker Sustainability Solutions device recall (Cls II)

    Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker Sustainability Solution Color Cuff 18" (Red), Quick Connect Dual Port Single Bladder REF 5921-018-135 Stryker Sustainability Solution Color Cuff 18" (Red) Dual Port Single Bladder REF 5921-018-235. — Reason: Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 12, 2026grant157d agoTUFTS UNIVERSITY BOSTON — Role of adipocyte interferon regulatory factor 8 in adipocyte and systemic me...

    DK grant. $232,000. PI: ANDREW S GREENBERG

    full page →nih reporter ↗
    ›Mar 12, 2026grant157d agoUNIVERSITY OF KENTUCKY — Targeting Intracellular Cholesterol Distribution: Mechanisms and Therapeutic ...

    DK grant. $707,062. PI: Xu Xiao

    full page →nih reporter ↗
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