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14,286 catalysts · 3,368 8k filing · 2,402 grant · 2,350 approval · 1,681 device 510k · 1,204 device recall · 1,151 device pma

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  • 8k filing3,368
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  • approval2,350
  • device 510k1,681
  • device recall1,204
  • device pma1,151
device adverse event
1,000
  • earnings584
  • recall465
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    Week of Nov 10, 2025

    6
    ›Nov 14, 2025device recall277d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE Lithotripsy System - Reusable Probes Model/Catalog Number: SPL-SR Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris. The ShockPulse transducer is a reusable device that requires cleaning and steam sterilization prior to use in order to generate both low-frequency mechanical impacts and high-frequency ultrasonic energy that quickly disintegrates stones. — Reason: Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the transducer plug and/or generator receptacle may cause these issues. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 14, 2025device recall277d agoAVID Medical, Inc. device recall (Cls II)AVITA Medical, Inc.

    Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10. — Reason: Potential for incomplete seal on header bag. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 14, 2025device recall277d agoGE Medical Systems China Co., Ltd. device recall (Cls I)

    GE Healthcare Carestation anesthesia system Power Management Board (PMB) Field Replaceable Unit (FRU), 2076139-001-S — Reason: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure. Anesthesia systems only operate on battery power in a rare event that AC mains power is lost and there is no continuous backup emergency power. If AC power is interrupted, the system will not automatically switch over to the battery supply mode and will reboot. If this issue occurs, a temporary disruption of mechanical ventilation, manual ventilation, and volatile agent delivery may occur. Following the reboot, the system will not return to the previous ventilation settings. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 14, 2025device recall277d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE Lithotripsy System - Single Use Probes Model/Catalog Number: SPL-S Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris. The ShockPulse transducer is a reusable device that requires cleaning and steam sterilization prior to use in order to generate both low-frequency mechanical impacts and high-frequency ultrasonic energy that quickly disintegrates stones. — Reason: Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the transducer plug and/or generator receptacle may cause these issues. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 16, 2025grant275d agoYALE UNIVERSITY — Defining a mechanism for inner nuclear membrane protein SUN2's mechanical reg...

    AR grant. $49,538. PI: Sandra Del Carmen Sandria

    full page →nih reporter ↗
    ›Nov 16, 2025grant275d agoMASSACHUSETTS INSTITUTE OF TECHNOLOGY — Deracemization of Beta2- and Gamma2-amino acids

    GM grant. $75,052. PI: Shivaani Sanjay Gandhi

    full page →nih reporter ↗

    Week of Nov 17, 2025

    44
    ›Nov 17, 2025approval274d agoOXYMORPHONE HYDROCHLORIDE — FDA approvalOXYMORPHONE HYDROCHLORIDE

    Sponsor: EPIC PHARMA LLC. Form: TABLET. Route: ORAL

    full page →OXYMORPHONE HYDROCHLORIDE →fda approvals ↗
    ›Nov 17, 2025approval
    ← prev
    page 36 of 286
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    274d ago
    TECENTRIQ HYBREZA (ATEZOLIZUMAB AND HYALURONIDASE-TQJS) — FDA approval(atezolizumab + hyaluronidase (human recombinant))

    Sponsor: GENENTECH INC. Form: INJECTABLE. Route: INJECTION

    full page →(atezolizumab + hyaluronidase (human recombinant)) →fda approvals ↗
    ›Nov 17, 2025approval274d agoLOPERAMIDE HYDROCHLORIDE — FDA approvalLOPERAMIDE HYDROCHLORIDE

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

    full page →LOPERAMIDE HYDROCHLORIDE →fda approvals ↗
    ›Nov 17, 2025approval274d agoTOFACITINIB CITRATE — FDA approvaltofacitinib citrate ER

    Sponsor: BIOCON PHARMA. Form: TABLET, EXTENDED RELEASE. Route: ORAL

    full page →tofacitinib citrate ER →fda approvals ↗
    ›Nov 17, 2025approval274d agoONDANSETRON HYDROCHLORIDE — FDA approvalondansetron hydrochloride CR

    Sponsor: GLAND PHARMA LTD. Form: INJECTABLE. Route: INJECTION

    full page →ondansetron hydrochloride CR →fda approvals ↗
    ›Nov 17, 2025approval274d agoMEMBRANEBLUE (TRYPAN BLUE) — FDA approval

    Sponsor: DORC. Form: SOLUTION. Route: OPHTHALMIC

    full page →fda approvals ↗
    ›Nov 17, 2025approval274d agoONDANSETRON — FDA approvalondansetron ODT

    Sponsor: SANDOZ. Form: TABLET, ORALLY DISINTEGRATING. Route: ORAL

    full page →ondansetron ODT →fda approvals ↗
    ›Nov 17, 2025approval274d agoTECENTRIQ (ATEZOLIZUMAB) — FDA approvalatezolizumab

    Sponsor: GENENTECH INC. Form: INJECTABLE. Route: INJECTION

    full page →atezolizumab →fda approvals ↗
    ›Nov 17, 2025approval274d agoPANRETIN (ALITRETINOIN) — FDA approvalalitretinoin

    Sponsor: ADVANZ PHARMA. Form: GEL. Route: TOPICAL

    full page →alitretinoin →fda approvals ↗
    ›Nov 17, 2025approval274d agoONDANSETRON HYDROCHLORIDE — FDA approvalondansetron hydrochloride CR

    Sponsor: GLAND PHARMA LTD. Form: INJECTABLE. Route: INJECTION

    full page →ondansetron hydrochloride CR →fda approvals ↗
    ›Nov 17, 2025approval274d agoNATACYN (NATAMYCIN) — FDA approvalHARROW, INC.

    Sponsor: HARROW EYE. Form: SUSPENSION. Route: OPHTHALMIC

    full page →fda approvals ↗
    ›Nov 17, 2025device 510k274d agoPiccolo Medical, Inc. — PM2™ System with ECGuide™ Connector (510k cleared)Picard Medical, Inc.

    Product code: LJS. Advisory committee: General Hospital. Type: Special

    full page →fda device 510k ↗
    ›Nov 17, 2025device 510k274d agoNobel Biocare C/O Medicim NV — DTX Studio Assist (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 17, 2025device 510k274d agoSiemens Medical Solutions USA, Inc. — ACUSON Maple Diagnostic Ultrasound System; ACUSON Maple Select Diagnostic Ultrasound System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 17, 2025device 510k274d agoMercator Medical (Thailand), Ltd. — Powder Free Nitrile Patient Examination Glove, Blue colored, Non-sterile Tested for Use with Chemotherapy Drugs and Fentanyl Citrate; Powder Free Nitrile Patient Examination Glove, Black colored, Non-sterile Tested for Use with Chemotherapy Drugs and Fentanyl Citrate (510k cleared)Teva Pharmaceuticals USA Inc

    Product code: LZA. Advisory committee: General Hospital. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 17, 2025device 510k274d agoBeckman Coulter, Inc. — Access Rubella IgG (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 17, 2025device 510k274d agoStarmed Co., Ltd. — TS-RF Generator (STS10) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 17, 2025device 510k274d agoNox Medical Ehf — DeepRESP (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 17, 2025device recall274d agoETAC A/S device recall (Cls II)

    Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory to mobile hoists) Model/Catalog Number: 1430116,1430117,1430115 Product Description: The mobile hoist is an assistive device intended for alleviation of, or compensation for, a functional, impairment due to an injury or disability. The device is designed for an individual lacking the ability to stand up and transfer themselves to / from a bed, the floor, a wheelchair, a chair, a toilet or similar due to reduced mobility or physical strength. — Reason: A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 17, 2025device recall274d agoSophysa device recall (Cls II)

    The Pressio 2 ICP Monitoring System, Model Number PSO-4000; Intracranial Pressure Monitor — Reason: Customer complaints of Pressio monitor rebooting. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 17, 2025device recall274d agoETAC A/S device recall (Cls II)

    Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: (1) M14000, (2) M1401, (3) M1402, (4) M14050, (5) M14150, (6) M1402-01, (7) M14050-00 (8) M14001; — Reason: A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 17, 2025device recall274d agoSheathing Technologies Inc device recall (Cls II)SPX Technologies, Inc.

    Sheathes3D Seamless Viral Barrier, Latex-Free, 7/8"D Tapered to 2.9"W x 11.8"L (2.2cm Tapered to 7.4cm x 30cm), Non-Sterile, Ultrasound Probe Cover, Vaginal/Rectal, Tapered, Rolled, Extra-Long, Individually Wrapped, Box of 50 Item Number 76339, — Reason: Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 17, 2025device recall274d agoSEASPINE ORTHOPEDICS CORPORATION device recall (Cls II)

    Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012; Navigation Straight Bone Probe, REF: PC2-400013; Navigation, 3.5mm Drill, REF: PC2-400135; Navigation, 4.0mm Drill, REF: PC2-400140; Navigation, 4.5mm Drill, PC2-400145; Navigation, 5.5mm Drill, REF: PC2-400155; Navigation, 3.5mm Tap, REF: PC2-400235; Navigation, 4.0mm Tap, REF: PC2-400240; Navigation, 4.5mm Tap, REF: PC2-400245; Navigation, 4.5mm Dual Lead Tap, REF: PC2-400345; Navigation, 5.5mm Dual Lead Tap, REF: PC2-400355 — Reason: The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards as compatible with the NorthStar OCT Navigation Instruments. However, the NorthStar OCT Navigation Instruments are compatible for use with Medtronic s Solera toolcards only. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 17, 2025device recall274d agoIntuitive Surgical, Inc. device recall (Cls II)INTUITIVE SURGICAL INC

    Da Vinci 5 ASSY, DV5 CONSOLE, IS5000 Model/Catalog Number: 380730 Used for minimally invasive surgery. — Reason: An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or tower monitor. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 17, 2025device recall274d agoETAC A/S device recall (Cls II)

    Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory to mobile hoists) Model/Catalog Numbers: (1) 1530101, (2) 1530102 Product Description: The mobile hoist is an assistive device intended for alleviation of, or compensation for, a functional, impairment due to an injury or disability. The device is designed for an individual lacking the ability to stand up and transfer themselves to / from a bed, the floor, a wheelchair, a chair, a toilet or similar due to reduced mobility or physical strength. — Reason: A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 17, 2025device recall274d agoETAC A/S device recall (Cls II)

    Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers: (1) M1501, (2) M1502, (3) M1504, (4) M15050, (5) M15151, (6) M15001, (7) M15002; Product Description: The mobile hoist is an assistive device intended for alleviation of, or compensation for, a functional, impairment due to an injury or disability. The device is designed for an individual lacking the ability to stand up and transfer themselves to / from a bed, the floor, a wheelchair, a chair, a toilet or similar due to reduced mobility or physical strength. Component: The deformation occurs between the bolt and the fork in the joint connecting the lifting bar and the arm on the Molift Mover. — Reason: A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 17, 2025grant274d agoUNIVERSITY OF CALIFORNIA BERKELEY — Site-Selective C-H Borylation Directed by Noncovalent Interactions

    GM grant. $74,632. PI: Jingyi Luo

    full page →nih reporter ↗
    ›Nov 17, 2025grant274d agoEMORY UNIVERSITY — The Nerve of Chemo: Unpacking Chemotherapy-Induced Peripheral Neuropathy in B...Emory University

    NR grant. $49,538. PI: La-Urshalar Beaushenique Brock

    full page →nih reporter ↗
    ›Nov 17, 2025grant274d agoPURDUE UNIVERSITY — Determining the Role of csoS2 in Carboxysome Assembly and Regulation

    GM grant. $75,052. PI: Kristy Rochon

    full page →nih reporter ↗
    ›Nov 18, 2025approval273d agoEPKINLY (EPCORITAMAB-BYSP) — FDA approvalepcoritamab

    Sponsor: GENMAB US, INC.. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →epcoritamab →fda approvals ↗
    ›Nov 18, 2025approval273d agoNALBUPHINE HYDROCHLORIDE — FDA approvalNALBUPHINE HYDROCHLORIDE

    Sponsor: RISING. Form: SOLUTION. Route: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    full page →NALBUPHINE HYDROCHLORIDE →fda approvals ↗
    ›Nov 18, 2025approval273d agoDICHLORPHENAMIDE — FDA approvalDICHLORPHENAMIDE

    Sponsor: RISING. Form: TABLET. Route: ORAL

    full page →DICHLORPHENAMIDE →fda approvals ↗
    ›Nov 18, 2025approval273d agoTAMSULOSIN HYDROCHLORIDE — FDA approvalTAMSULOSIN HYDROCHLORIDE

    Sponsor: ASCENT PHARMS INC. Form: CAPSULE. Route: ORAL

    full page →TAMSULOSIN HYDROCHLORIDE →fda approvals ↗
    ›Nov 18, 2025approval273d agoFLUPHENAZINE HYDROCHLORIDE — FDA approvalFLUPHENAZINE HYDROCHLORIDE

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

    full page →FLUPHENAZINE HYDROCHLORIDE →fda approvals ↗
    ›Nov 18, 2025approval273d agoNIZORAL ANTI-DANDRUFF (KETOCONAZOLE) — FDA approvalTeva Pharmaceuticals USA Inc

    Sponsor: KRAMER. Form: SHAMPOO. Route: TOPICAL

    full page →fda approvals ↗
    ›Nov 18, 2025approval273d agoPYZCHIVA (USTEKINUMAB-TTWE) — FDA approvalPYZCHIVA

    Sponsor: SAMSUNG BIOEPIS CO LTD. Form: INJECTABLE. Route: INJECTION

    full page →PYZCHIVA →fda approvals ↗
    ›Nov 18, 2025approval273d agoPYZCHIVA (USTEKINUMAB-TTWE) — FDA approvalPYZCHIVA

    Sponsor: SAMSUNG BIOEPIS CO LTD. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →PYZCHIVA →fda approvals ↗
    ›Nov 18, 2025approval273d agoONDANSETRON HYDROCHLORIDE — FDA approvalondansetron hydrochloride CR

    Sponsor: HOSPIRA. Form: INJECTABLE. Route: INJECTION

    full page →ondansetron hydrochloride CR →fda approvals ↗
    ›Nov 18, 2025approval273d agoSUPREP BOWEL PREP KIT (MAGNESIUM SULFATE) — FDA approvalMAGNESIUM SULFATE

    Sponsor: AZURITY. Form: SOLUTION. Route: ORAL

    full page →MAGNESIUM SULFATE →fda approvals ↗
    ›Nov 18, 2025approval273d agoONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE (ONDANSETRON HYDROCHLORIDE) — FDA approvalondansetron hydrochloride CR

    Sponsor: HOSPIRA. Form: INJECTABLE. Route: INJECTION

    full page →ondansetron hydrochloride CR →fda approvals ↗
    ›Nov 18, 2025approval273d agoREDEMPLO (PLOZASIRAN SODIUM) — FDA approvalplozasiran sodium

    Sponsor: ARROWHEAD. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →plozasiran sodium →fda approvals ↗
    ›Nov 18, 2025device 510k273d agoGuangzhou Wondfo Biotech Co., Ltd. — SAFElife T-Cup Multi-Drug Urine Test Cup; SAFElife T-Cup Multi-Drug Urine Test Cup Dx (510k cleared)

    Product code: NFT. Advisory committee: Clinical Toxicology. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 18, 2025device 510k273d agoCollagen Matrix, Inc. — Collagen Dura Regeneration Membrane - Repair (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 18, 2025device 510k273d agoUlrich GmbH & Co. KG — ulricheasyINJECT Max 2M (XD 10140); ulricheasyINJECT Max 3 (XD 10150); ulricheasyINJECT Max 3 (XD 10180) (510k cleared)

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

    full page →fda device 510k ↗
    $RCEL7.8500-2.00%
    $PMI0.1821-4.66%
    $SPXC217.32+2.43%
    $ARWR86.64+1.23%
    $ISRG394.51-1.68%
    $HROW40.03+2.98%