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19,834 catalysts · 4,728 grant · 3,277 8k filing · 2,785 device 510k · 2,724 approval · 2,000 device recall · 1,962 device pma

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  • grant4,728
  • 8k filing3,277
  • device 510k2,785
  • approval2,724
  • device recall2,000
  • device pma1,962
device adverse event
1,000
  • recall693
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Jul 14, 2025

    50
    ›Jul 17, 2025device pma393d agoMedtronic, Inc. — Activa™ Deep Brain Stimulation Therapy System, Percept™ PC BrainSense™ (PMA supplement)Medtronic plc

    Supplement type: 30-Day Notice. Product code: MHY. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Jul 17, 2025device pma393d agoMedtronic Neuromodulation — InterStim™ Therapy System, Verify™ Evaluation System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: EZW. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Jul 17, 2025device pma393d agoMedtronic Neuromodulation — InterStim™ Therapy System, Verify™ Evaluation System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: QON. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Jul 17, 2025device pma393d agoMedtronic Vascular, Inc. — Protégé™ RX Carotid Stent System (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: NIM. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Jul 17, 2025device pma393d agoMedtronic, Inc. — Activa® Deep Brain Stimulation Therapy System, Percept™ PC BrainSense™ (PMA supplement)Medtronic plc

    Supplement type: 30-Day Notice. Product code: MHY. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Jul 17, 2025device pma393d agoMedtronic, Inc. — SynchroMed® Infusion System, Ascenda® Intrathecal Catheters (PMA supplement)Medtronic plc

    Supplement type: 30-Day Notice. Product code: LKK. Advisory committee: HO. Decision: OK30

    full page →fda device pma ↗
    ›Jul 17, 2025device pma393d agoMedtronic, Inc. — SynchroMed™ Infusion System, Ascenda™ Intrathecal Catheters (PMA supplement)Medtronic plc

    Supplement type: 30-Day Notice. Product code: LKK. Advisory committee: HO. Decision: OK30

    full page →fda device pma ↗
    ›Jul 17, 2025device recall393d agoC.R. Bard Inc device recall (Cls II)

    SureStep Foley Tray System Bardex I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303316A — Reason: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone hydrogel with antimicrobial coating, or 3)Natural latex with infection control, when it's silicone hydrogel coated without antimicrobial coating, which may cause infection and/or local and/or systemic allergic reaction — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 17, 2025device recall393d agoC.R. Bard Inc device recall (Cls II)

    SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303414A — Reason: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone hydrogel with antimicrobial coating, or 3)Natural latex with infection control, when it's silicone hydrogel coated without antimicrobial coating, which may cause infection and/or local and/or systemic allergic reaction — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 17, 2025device recall393d agoQuest International, Inc. device recall (Cls II)QDM International Inc.

    Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked Immunoabsorbant Assay, Rubeola IgM Model/Catalog Number: 01-190M Software Version: N/A Product Description: Measles IgM tests, performed using ELISA (Enzyme-Linked Immunosorbent Assay) method, used to detect the presence of IgM antibodies against measles virus in a patient's serum or plasma Component: not a component — Reason: Measles IgM Test Kit lacks premarket approval or clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 17, 2025device recall393d agoMedtronic Xomed, Inc. device recall (Cls II)Medtronic USA Inc

    IPC Powerease System REF 2300000 UDI-DI: 00613994448705 00643169406834. The IPC POWEREASE System is indicated for drilling, tapping, and driving screws and working end attachments during spinal surgery, including open and minimally invasive procedures. The IPC POWEREASE System is also used in the placement of screws, or cutting of screws, posts, and rods. The IPC is indicated for the incision/cutting, removal, drilling, and sawing of soft and hard tissue and bone, and biomaterials in Neurosurgical (Cranial, Craniofacial), Orthopedic, Arthroscopic, Spinal, Sternotomy, and General surgical procedures. — Reason: Due to out of the box wobble of the driver. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 17, 2025device recall393d agoC.R. Bard Inc device recall (Cls II)

    SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray, REF: A942216 — Reason: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone hydrogel with antimicrobial coating, or 3)Natural latex with infection control, when it's silicone hydrogel coated without antimicrobial coating, which may cause infection and/or local and/or systemic allergic reaction — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 17, 2025device recall393d agoO&M HALYARD INC device recall (Cls II)

    Orthopedic Pack, Model: 88041-12 AC2424601B 09/02/2029 Universal Pack, Model: 77165-06 AC2424902B 09/05/2029 — Reason: Surgical drape packs may have open seals, which may compromise the sterility of the product. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 17, 2025device recall393d agoPhilips Medical Systems (Cleveland) Inc device recall (Cls II)

    Pinnacle 3 with TumorLOC, (870258) Radiation Therapy Planning System Software — Reason: Due to software issue, Radiation Therapy Planning system may provide incorrect dataset calculations when performing the "Stopping Power Ratio" (SPR) , — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 17, 2025device 510k393d agoRoche Diagnostics — Elecsys Cortisol III (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 17, 2025device 510k393d agoGeistlich Pharma AG — Device 300423 Granules (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 17, 2025device 510k393d agoDxtx Medical, Inc. — e2CoilTM Imaging System for the Siemens MAGNETOM 3.0T MRI Systems with Tim 4G Connector (510k cleared)ICU MEDICAL INC/DE

    Product code: MOS. Advisory committee: Radiology. Type: Abbreviated

    full page →fda device 510k ↗
    ›Jul 17, 2025device 510k393d agoTerumo Corporation — DualView Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 17, 2025device 510k393d agoMasimo Corporation — Masimo O3 Regional Oximeter (510k cleared)MASIMO CORP

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

    full page →fda device 510k ↗
    ›Jul 17, 2025device 510k393d agoAlafair Biosciences — VersaWrap Nerve Protector (VTP-2201); VersaWrap Nerve Protector (VTP-1201) (510k cleared)

    Product code: JXI. Advisory committee: Neurology. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 17, 2025device 510k393d agoMedacta International S.A. — MectaLIF 3D Metal (510k cleared)Stemedica International S.A.

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

    full page →fda device 510k ↗
    ›Jul 17, 2025device 510k393d agoOsstem Implant Company., Ltd. Chair Business — K5 Cart, K5 Mount, K5 Swing (510k cleared)

    Product code: EIA. Advisory committee: Dental. Type: Special

    full page →fda device 510k ↗
    ›Jul 17, 2025device 510k393d agoArbor Endovascular, LLC — 0.014” Willow Guidewire (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 17, 2025device 510k393d agoShanghai United Imaging Healthcare Co., Ltd. — uMR Ultra (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 17, 2025device 510k393d agoShanghai United Imaging Healthcare Co., Ltd. — uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 17, 2025device 510k393d agoGenoray Co., Ltd. — HESTIA (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 18, 2025approval392d agoZEJULA (NIRAPARIB TOSYLATE) — FDA approvalniraparib

    Sponsor: GLAXOSMITHKLINE. Form: TABLET. Route: ORAL

    full page →niraparib →fda approvals ↗
    ›Jul 18, 2025device pma392d agoExact Sciences Corporation — Cologuard® (PMA supplement)

    Supplement type: Real-Time Process. Product code: PHP. Advisory committee: PA. Decision: APPR

    full page →fda device pma ↗
    ›Jul 18, 2025device pma392d agoExact Sciences Corporation — Cologuard Plus™ (PMA supplement)

    Supplement type: Real-Time Process. Product code: PHP. Advisory committee: PA. Decision: APPR

    full page →fda device pma ↗
    ›Jul 18, 2025device pma392d agoBerlin Heart, Inc. — EXCOR Pediatric Ventricular Assist Device (PMA supplement)

    Supplement type: Real-Time Process. Product code: DSQ. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Jul 18, 2025device pma392d agoFerrosan Meidcal Devices A/S — SURGIFLO® Hemostatic Matrix; SURGIFLO® Hemostatic Matrix Kit with Thrombin (PMA supplement)PFIZER INC

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

    full page →fda device pma ↗
    ›Jul 18, 2025device pma392d agoPhraxis, Inc. — EndoForce™ Connector for Endovascular Venous Anastomosis (PMA supplement)

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

    full page →fda device pma ↗
    ›Jul 18, 2025device pma392d agoOrganox Limited — OrganOx metra® System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: QQK. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Jul 18, 2025device pma392d agoAlcon Laboratories, LLC — Clareon Aspheric Hydrophobic Acrylic Intraocular Lens (IOL), Clareon ToricAspheric Hydrophobic Acrylic Intraocular Lens, (PMA supplement)Alcon Laboratories Inc

    Supplement type: 30-Day Notice. Product code: HQL. Advisory committee: OP. Decision: OK30

    full page →fda device pma ↗
    ›Jul 18, 2025device pma392d agoDepuy, Inc. — LCS(R) TOTAL KNEE SYSTEM (PMA supplement)

    Supplement type: 135 Review Track For 30-Day Notice. Product code: NJL. Advisory committee: OR. Decision: APPR

    full page →fda device pma ↗
    ›Jul 18, 2025device recall392d agoEncore Medical, LP device recall (Cls II)Encore Medical, Inc.

    Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER BOSS DRILL, 6.5mm Model/Catalog Number: 804-06-312 Product Description: Material: S.S., Non Sterile — Reason: Their is a potential that the reamer may kick or bind up during or immediately prior to use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 18, 2025device recall392d agoEncore Medical, LP device recall (Cls II)Encore Medical, Inc.

    Brand Name: DJO SURGICAL Product Name: FA S Altivate Reverse Glenoid Tray Model/Catalog Number: None Software Version: NA Product Description: Enovis" shoulder devices are intended for treatment of patients who are candidates for shoulder arthroplasty per the Indication for use. While total shoulder replacements are not intended to withstand activity levels and loads of normal healthy bone, they are a means of restoring mobility and reducing pain for many patients. The AltiVate Reverse¿ Shoulder Prosthesis is indicated as a reverse shoulder replacement for patients with a functional deltoid muscle and a grossly deficient rotator cuff joint suffering from pain and dysfunction due to: " Severe arthropathy with a grossly deficient rotator cuff; " Previously failed joint replacement with a grossly deficient rotator cuff; " Fracture of glenohumeral joint from trauma or pathologic conditions of the shoulder including humeral head fracture, displaced 3- or 4-part fractures of proximal humerus, or reconstruction after tumor resection; " Bone defect in proximal humerus; " Non-inflammatory degenerative disease including osteoarthritis and avascular necrosis of the natural humeral head and/or glenoid; " Inflammatory arthritis including rheumatoid arthritis; " Correction of functional deformity. The glenoid baseplate is intended for cementless application with addition of screws for fixation. This device may also be indicated in the salvage of previously failed surgical attempts for anatomic and hemi procedures. All RSP¿ Monoblock and AltiVate Reverse¿ humeral stems are intended for cemented or cementless use. Enovis" instrumentation consists of devices and their accessories used in surgical procedures. Implantation of Enovis" products should only be performed with Enovis" instrumentation or instrumentation distributed by Enovis". Enovis" instruments and instrument cases are generally composed of titanium, stainless steel, aluminum, and/or polymeric materials. The cases may be multi-layered with various inserts to hold surgical instrumentation in place during handling and storage. The inserts may consist of trays, holders, and silicone mats. The instrument cases will allow sterilization of the contents to occur in a steam autoclave utilizing the cleaning, sterilization, and drying cycle that has been validated and detailed below. Instrument cases do not provide a sterile barrier and must be used in conjunction with FDA cleared sterilization wrap to maintain sterility. Instruments are provided non-sterile and should be stored in their original packaging until cleaned and sterilized according to the recommended guidelines listed below. Component: NA — Reason: Their is a potential that the reamer may kick or bind up during or immediately prior to use. — Status: Ongoing

    ›Jul 18, 2025device recall392d agoEncore Medical, LP device recall (Cls II)Encore Medical, Inc.

    Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD Model/Catalog Number: 804-06-311 Product Description: Material: S.S/Nitronic, Non-Sterile — Reason: Their is a potential that the reamer may kick or bind up during or immediately prior to use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 18, 2025device recall392d agoEncore Medical, LP device recall (Cls II)Encore Medical, Inc.

    Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER SLEEVE Model/Catalog Number: 804-06-310 Product Description: Material: S.S/CoCrMo, Non-Sterile — Reason: Their is a potential that the reamer may kick or bind up during or immediately prior to use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 18, 2025device 510k392d agoZimmer, Inc. — Z1 Hip System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 18, 2025device 510k392d agoHeartFlow, Inc. — HeartFlow Analysis (510k cleared)Heartflow, Inc.

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

    full page →fda device 510k ↗
    ›Jul 18, 2025device 510k392d agoDk Medical Systems Co., Ltd. — INNOVISION-P5 (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 18, 2025device 510k392d agoMicro Current Technology, Inc. — MF SC GEN2 Facial Toning System (510k cleared)MICRON TECHNOLOGY INC

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

    full page →fda device 510k ↗
    ›Jul 18, 2025device 510k392d agoExcite Medical of Tampa Bay, LLC — True Non-Surgical Spinal Decompression System (DRX9000-SL) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 18, 2025device 510k392d agoBeckman Coulter, Inc. — MicroScan Dried Gram-Negative MIC/Combo Panels with Aztreonam (AZT) (0.5-64 µg/mL) (510k cleared)Bristol-Myers Squibb Co

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

    full page →fda device 510k ↗
    ›Jul 18, 2025device 510k392d agoCMT Health PTE., Ltd. — Profoject™ Enteral Feeding Syringe (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 18, 2025device 510k392d agoStryker Endoscopy — SPY Cystoscope/Hysteroscope (510k cleared)

    Product code: HIH. Advisory committee: Obstetrics/Gynecology. Type: Special

    full page →fda device 510k ↗
    ›Jul 18, 2025device 510k392d agoArthrex, Inc. — Arthrex FiberTak Suture Anchor (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 18, 2025device 510k392d agoTomey Corporation — Tomey Cornea/Anterior Segment OCT (CASIA2) (510k cleared)

    Product code: OBO. Advisory committee: Ophthalmic. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 18, 2025device 510k392d agoAlafair Biosciences — VersaCoat Tendon Protector (VTP-44G2); VersaCoat Tendon Protector (VTP-12G1) (510k cleared)

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

    full page →fda device 510k ↗
    ← prev
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    full page →fda device recalls ↗
    $MDT91.10+0.37%
    $QDMI
    $MASI
    $EMI
    $ICUI180.90+0.87%
    $EMI
    $PFE26.86+2.11%
    $MDT91.10+0.37%
    $MDT91.10+0.37%
    $MDT91.10+0.37%
    $EMI
    $EMI
    $HTFL
    $MU973.67+6.85%