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10,070 catalysts · 3,350 8k filing · 2,079 grant · 1,097 approval · 1,000 device adverse event · 800 device 510k · 584 earnings

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  • 8k filing3,350
  • grant2,079
  • approval1,097
  • device adverse event1,000
  • device 510k800
  • earnings584
device pma
573
  • device recall291
  • recall215
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Jan 26, 2026

    50
    ›Jan 26, 2026approval202d agoBUDESONIDE — FDA approvalbudesonide DR

    Sponsor: RISING. Form: CAPSULE, DELAYED RELEASE. Route: ORAL

    full page →budesonide DR →fda approvals ↗
    ›Jan 26, 2026approval202d agoQUIOFIC (FOLIC ACID) — FDA approvalfolic acid

    Sponsor: SOLUBIOMIX. Form: SOLUTION. Route: ORAL

    full page →folic acid →fda approvals ↗
    ›Jan 26, 2026approval202d agoCUPRIC CHLORIDE — FDA approvalCUPRIC CHLORIDE

    Sponsor: AMNEAL. Form: INJECTABLE. Route: INJECTION

    full page →CUPRIC CHLORIDE →fda approvals ↗
    ›Jan 26, 2026device 510k202d agoOutset Medical, Inc. — Tablo Hemodialysis System (PN-0008000, PN-0006000U) (510k cleared)Outset Medical, Inc.

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

    full page →fda device 510k ↗
    ›Jan 26, 2026device 510k202d agoEyas Medical Imaging, Inc. — Ascent3T Neonatal Magnetic Resonance Imaging System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 26, 2026device 510k202d agoGe Medical Systems Information Technologies, Inc. — MAC 7 Resting ECG Analysis System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 26, 2026device pma202d agoDiaSorin, Inc. — LIAISON QuantiFERON TB Gold Plus II; LIAISON Control QuantiFERON TB Gold Plus II (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: NCD. Advisory committee: MI. Decision: APPR

    full page →fda device pma ↗
    ›Jan 26, 2026device recall202d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 26, 2026device recall202d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 26, 2026device recall202d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 26, 2026device recall202d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 5 M12 System Model Numbers: (1)722227, (2)722231; Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 26, 2026device recall202d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230, (4)722280(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 26, 2026device recall202d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229; Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 26, 2026device recall202d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236; Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 26, 2026device recall202d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 5 M20 System Model Numbers: (1)722228, (2)722232, (3)722281(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 26, 2026grant202d agoFLORIDA INTERNATIONAL UNIVERSITY — CRISPR/dCas9-Targeted Histone Demethylation Interplays with DNA Repair to Con...

    NS grant. $1,319,674. PI: Prem P Chapagain

    full page →nih reporter ↗
    ›Jan 26, 2026grant202d agoEMORY UNIVERSITY — Neuromodulation of somato-sympathetic postganglionic activity after SCIEmory University

    NS grant. $234,750. PI: SHAWN HOCHMAN

    full page →nih reporter ↗
    ›Jan 27, 2026approval201d agoDARZALEX FASPRO (DARATUMUMAB AND HYALURONIDASE-FIHJ) — FDA approval(daratumumab + hyaluronidase (human recombinant))

    Sponsor: JANSSEN BIOTECH. Form: INJECTABLE. Route: INJECTION

    full page →(daratumumab + hyaluronidase (human recombinant)) →fda approvals ↗
    ›Jan 27, 2026approval201d agoNOXAFIL POWDERMIX KIT (POSACONAZOLE) — FDA approvalPOSACONAZOLE

    Sponsor: MSD MERCK CO. Form: FOR SUSPENSION, DELAYED RELEASE. Route: ORAL

    full page →POSACONAZOLE →fda approvals ↗
    ›Jan 27, 2026approval201d agoTAPENTADOL HYDROCHLORIDE — FDA approvalCOLLEGIUM PHARMACEUTICAL, INC

    Sponsor: HUMANWELL. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Jan 27, 2026approval201d agoNOXAFIL (POSACONAZOLE) — FDA approvalPOSACONAZOLE

    Sponsor: MERCK SHARP DOHME. Form: SOLUTION. Route: INTRAVENOUS

    full page →POSACONAZOLE →fda approvals ↗
    ›Jan 27, 2026approval201d agoFIDAXOMICIN — FDA approvalDificid

    Sponsor: TORRENT. Form: TABLET. Route: ORAL

    full page →Dificid →fda approvals ↗
    ›Jan 27, 2026approval201d agoVYXEOS (CYTARABINE) — FDA approvalMeitheal Pharmaceuticals Inc

    Sponsor: JAZZ PHARMS THERAP. Form: POWDER. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Jan 27, 2026approval201d agoMESNA — FDA approvalRiconpharma LLC

    Sponsor: EUGIA PHARMA. Form: INJECTABLE. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Jan 27, 2026approval201d agoTOPIRAMATE — FDA approvaltopiramate ER

    Sponsor: NATCO. Form: TABLET. Route: ORAL

    full page →topiramate ER →fda approvals ↗
    ›Jan 27, 2026approval201d agoPROPRANOLOL HYDROCHLORIDE — FDA approvalpropranolol hydrochloride ER

    Sponsor: MANKIND PHARMA. Form: TABLET. Route: ORAL

    full page →propranolol hydrochloride ER →fda approvals ↗
    ›Jan 27, 2026approval201d agoIDOSE TR (TRAVOPROST) — FDA approvalTRAVOPROST

    Sponsor: GLAUKOS. Form: IMPLANT. Route: INTRACAMERAL

    full page →TRAVOPROST →fda approvals ↗
    ›Jan 27, 2026approval201d agoIDOSE TR (TRAVOPROST) — FDA approvalTRAVOPROST

    Sponsor: GLAUKOS. Form: IMPLANT. Route: INTRACAMERAL

    full page →TRAVOPROST →fda approvals ↗
    ›Jan 27, 2026approval201d agoNOXAFIL (POSACONAZOLE) — FDA approvali3 Pharmaceuticals LLC

    Sponsor: SCHERING. Form: SUSPENSION. Route: ORAL

    full page →fda approvals ↗
    ›Jan 27, 2026approval201d agoCAPECITABINE — FDA approvalArmas Pharmaceuticals Inc

    Sponsor: ALKEM LABS LTD. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Jan 27, 2026approval201d agoCAPRELSA (VANDETANIB) — FDA approvalvandetanib

    Sponsor: GENZYME CORP. Form: TABLET. Route: ORAL

    full page →vandetanib →fda approvals ↗
    ›Jan 27, 2026approval201d agoPRIFTIN (RIFAPENTINE) — FDA approvalrifapentine

    Sponsor: SANOFI AVENTIS US. Form: TABLET. Route: ORAL

    full page →rifapentine →fda approvals ↗
    ›Jan 27, 2026approval201d agoAMPICILLIN AND SULBACTAM (AMPICILLIN SODIUM) — FDA approvalUNASYN

    Sponsor: SANDOZ. Form: INJECTABLE. Route: INJECTION

    full page →UNASYN →fda approvals ↗
    ›Jan 27, 2026approval201d agoDEFLAZACORT — FDA approvalAmneal Pharmaceuticals, Inc.

    Sponsor: SUN PHARM INDS INC. Form: SUSPENSION. Route: ORAL

    full page →fda approvals ↗
    ›Jan 27, 2026approval201d agoNOXAFIL (POSACONAZOLE) — FDA approvalPOSACONAZOLE

    Sponsor: MERCK SHARP DOHME. Form: TABLET, DELAYED RELEASE. Route: ORAL

    full page →POSACONAZOLE →fda approvals ↗
    ›Jan 27, 2026device 510k201d agoSoniquence, LLC — Reusable 3 Button Fingerswitch Wand (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 27, 2026device 510k201d agoBalt USA, LLC — Optima Coil System (OptiOne Coil System) (510k cleared)Bayer USA LLC

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

    full page →fda device 510k ↗
    ›Jan 27, 2026device 510k201d agoInbella Medical, Inc. — InbellaIgnite RF System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 27, 2026device 510k201d agoBeckman Coulter, Inc. — Access anti-HAV IgM (510k cleared)

    Product code: LOL. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
    ›Jan 27, 2026device 510k201d agoAidoc Medical , Ltd. — BriefCase-Triage (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 27, 2026device pma201d agoBoston Scientific Corp — WOLVERINE™ Coronary Cutting Balloon™ (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Jan 27, 2026device pma201d agoMedtronic Vascular — Endurant Stent Graft System; Endurant II/IIs Stent Graft System; Endurant II AUI Stent Graft System (PMA supplement)

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

    full page →fda device pma ↗
    ›Jan 27, 2026device recall201d agoAbiomed, Inc. device recall (Cls I)Abion Inc

    Impella RP Flex with SmartAssist. Product Code: 1000323. — Reason: Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 27, 2026device recall201d agoAbiomed, Inc. device recall (Cls I)Abion Inc

    Impella RP with SmartAssist. Product Code: 0046-0035. — Reason: Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 27, 2026device recall201d agoAbiomed, Inc. device recall (Cls I)Abion Inc

    Impella RP. Product Code: 0046-0011. — Reason: Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 27, 2026device recall201d agoBecton Dickinson & Company device recall (Cls II)BECTON DICKINSON & CO

    10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case. — Reason: During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 27, 2026device recall201d agoLutronic Corporation device recall (Cls II)

    CLARITY II Laser System; Model No. 1110200210. — Reason: Reports of devices sparking/popping and potentially burning patients. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 27, 2026grant201d agoUNIVERSITY OF MINNESOTA — Testing the role of microbial infections in the development of auto-antibodie...University of Minnesota

    AI grant. $43,914. PI: Adrianna M. Rivera-León

    full page →nih reporter ↗
    ›Jan 27, 2026grant201d agoUNIVERSITY OF CALIFORNIA LOS ANGELES — Predicting ASD Outcomes Using Quantitative Movement Metrics in InfancyUniversity of California Los Angeles

    NS grant. $625,859. PI: Rujuta Bhatt Wilson

    full page →nih reporter ↗
    ›Jan 27, 2026grant201d agoALBERT EINSTEIN COLLEGE OF MEDICINE — Understanding how T cell receptor recognition of peptide ligands shapes memor...Albert Einstein College of Medicine

    AI grant. $780,787. PI: Gregoire Stephane Lauvau

    full page →nih reporter ↗
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