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calendar

14,126 catalysts · 3,208 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 filing3,208
  • grant2,402
  • approval2,350
  • device 510k1,681
  • device recall1,204
  • device pma1,151
device adverse event
1,000
  • earnings584
  • recall465
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Oct 6, 2025

    50
    ›Oct 6, 2025approval312d agoLITHIUM CARBONATE — FDA approvalCamber Pharmaceuticals Inc

    Sponsor: PHARMOBEDIENT. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Oct 6, 2025approval312d agoBUSPIRONE HYDROCHLORIDE — FDA approvalBUSPIRONE HYDROCHLORIDE

    Sponsor: RISING. Form: TABLET. Route: ORAL

    full page →BUSPIRONE HYDROCHLORIDE →fda approvals ↗
    ›Oct 6, 2025approval312d agoSALONPAS (MENTHOL) — FDA approvalHisamitsu America Inc

    Sponsor: HISAMITSU PHARM CO. Form: PATCH. Route: TOPICAL

    full page →fda approvals ↗
    ›Oct 6, 2025approval312d agoLITHIUM CARBONATE — FDA approvalCamber Pharmaceuticals Inc

    Sponsor: PHARMOBEDIENT. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Oct 6, 2025approval312d agoOLMESARTAN MEDOXOMIL, AMLODIPINE AND HYDROCHLOROTHIAZIDE (AMLODIPINE BESYLATE) — FDA approvalamlodipine besylate

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

    full page →amlodipine besylate →fda approvals ↗
    ›Oct 6, 2025device 510k312d agoPainchek Limited (Ltd.) — PainChek (PainChek Adult) (510k cleared)

    Product code: SGB. Advisory committee: Neurology. Type: Direct

    full page →fda device 510k ↗
    ›Oct 6, 2025device 510k312d agoZhejiang Topwe Tools Manufacturing Co.,Ltd — Wheelchair (N817) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 6, 2025device 510k312d agoColoplast Corp. — Heylo™ System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 6, 2025device 510k312d agoNanjing Kangni Smart Technology Co., Ltd. — Folding Mobility Scooter (KD101) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 6, 2025device 510k312d agoRapid Medical , Ltd. — Tigertriever 17 Ultra Revascularization Device (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 6, 2025device 510k312d agoDeep Breathe, Inc. — BlineSlide (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 6, 2025device 510k312d agoCovidien, LLC — Shiley™ Oral RAE Tracheal Tube Cuffless, Murphy Eye (113-XX) Shiley™ Nasal RAE Tracheal Tube Cuffless, Murphy Eye (114-XX) Shiley™ Oral RAE Tracheal Tube Cuffed, Murphy Eye (115-XX) Shiley™ Oral RAE Tracheal Tube with TaperGuard™ Cuff, Murphy Eye (115-XXOR) Shiley™ Nasal RAE Tracheal Tube with TaperGuard™ Cuff, Murphy Eye (119-XXNR) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 6, 2025device pma312d agoOphtec BV — Capsular Tension Ring (275,276); RingJect (375,376) (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 6, 2025device pma312d agoABBOTT MEDICAL — HeartMate 3™ Left Ventricular Assist System (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 6, 2025device pma312d agoEndotronix, Inc. — CorPASS System (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 6, 2025device recall312d agoApplied Medical Technology Inc device recall (Cls II)

    Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I — Reason: The nasal feeding tube may be occluded — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoSiemens Healthcare Diagnostics, Inc. device recall (Cls II)

    Food Panel 3 Specific Allergen; Siemens Material Number (SMN): 10385891; Catalog Number: FP3L4; — Reason: The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge. When using an IMMULITE 2000 / IMMULITE 2000 XPi instrument in combination with a Zebra barcode scanner, the instrument will not correctly recognize the position of tubes within the allergen holder wedge. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoAbbott Medical device recall (Cls II)

    Eterna SCS IPG (Implantable Pulse Generator), Model Number 32400 — Reason: There is a potential issue affecting Eterna Spinal Cord Stimulation (SCS) Implantable Pulse Generators (IPGs), Model 32400 and Liberta RC Deep Brain Stimulation (DBS) Implantable Pulse Generators (IPGs), Model 62400 . These devicess may experience a loss of communication with the Clinician Programmer (CP) and/or the Patient Controller (PC). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoPOLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC device recall (Cls III)

    OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials designed to monitor FOBT (Fecal Occult Blood Test) — Reason: A labeling error was identified on the affected product. The expiration date on the kit box label and on the vial labels incorrectly stated the expiration date as 2026-01-16. The correct expiration date should be 2027-01-17. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoAbbott Medical device recall (Cls II)

    Liberta RC DBS IPG (Implantable Pulse Generator), Model Number 62400 — Reason: There is a potential issue affecting Eterna Spinal Cord Stimulation (SCS) Implantable Pulse Generators (IPGs), Model 32400 and Liberta RC Deep Brain Stimulation (DBS) Implantable Pulse Generators (IPGs), Model 62400 . These devicess may experience a loss of communication with the Clinician Programmer (CP) and/or the Patient Controller (PC). — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoApplied Medical Technology Inc device recall (Cls II)

    Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06055-I — Reason: The nasal feeding tube may be occluded — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoApplied Medical Technology Inc device recall (Cls II)

    Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-I — Reason: The nasal feeding tube may be occluded — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400 Product Name: Single Use Single Use Electrosurgical Snare Model/Catalog Number: SD-U400U-15 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and/or cauterization of diminutive polyps, sessile polyps, pedunculated polyps, and tissue from within the GI tract. — Reason: Sterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf carton. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoApplied Medical Technology Inc device recall (Cls II)

    Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-N-I — Reason: The nasal feeding tube may be occluded — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoSiemens Healthcare Diagnostics, Inc. device recall (Cls II)

    3gAllergy Specific IgE Universal Kit; Kit Component: 3gAllergy Specific IgE Adjustor Antibody (L2UNS1), 3gAllergy Specific IgE Control Antibody (L2UNS2); Siemens Material Number (SMN): 10380875; Catalog Number: L2KUN6; — Reason: The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge. When using an IMMULITE 2000 / IMMULITE 2000 XPi instrument in combination with a Zebra barcode scanner, the instrument will not correctly recognize the position of tubes within the allergen holder wedge. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoSiemens Healthcare Diagnostics, Inc. device recall (Cls II)

    IMMULITE 2000 Oak Mix Specific Allergen; Siemens Material Number (SMN): 10386105; Catalog Number: L2KUN6; — Reason: The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge. When using an IMMULITE 2000 / IMMULITE 2000 XPi instrument in combination with a Zebra barcode scanner, the instrument will not correctly recognize the position of tubes within the allergen holder wedge. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus Single Use Electrosurgical Snare SD-400 Product Name: Single Use Electrosurgical Snare Model/Catalog Number: SD-400U-10 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and/or cauterization of diminutive polyps, sessile polyps, pedunculated polyps, and tissue from within the GI tract. — Reason: Sterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf carton. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoTandem Diabetes Care, Inc. device recall (Cls I)TANDEM DIABETES CARE INC

    Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize a motor-driven mechanism to deliver insulin from within a disposable cartridge, through an infusion set, into a patient s subcutaneous tissue. As with current insulin infusion pumps on the U.S. market, the desired timing and quantity of the insulin delivery is programmed by the user (i.e., the patient). Pump, Tandem Mobi, Control-IQ/1010750, Pump, Tandem Mobi, Control-IQ, Replacement/1012719, Pump, Tandem Mobi, Control-IQ 7.6.0.3, Medicare/1013501, Pump, Tandem Mobi, Control-IQ 7.7/1013655, Pump, Tandem Mobi, Control-IQ, 7.7, Replacement/1013656, Pump, Tandem Mobi, Control-IQ 7.7, Medicare/1013700, Pharmacy Kit, Starter Pack, Tandem Mobi 7.7/1014081 — Reason: Insulin pump includes a vibration motor that gives tactile feedback for any alerts, alarms, or malfunctions. Pump may exhibit false vibration motor failure due to a software issue causing Malfunction 12: "Pump cannot operate, the mobile app can no longer receive data from the pump. Insulin delivery and any active CGM Sessions have been stopped", which could result in hyperglycemia. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 6, 2025device recall312d agoApplied Medical Technology Inc device recall (Cls II)

    Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I — Reason: The nasal feeding tube may be occluded — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 7, 2025approval311d agoJASCAYD (NERANDOMILAST) — FDA approvalnerandomilast

    Sponsor: BOEHRINGER INGELHEIM. Form: TABLET. Route: ORAL

    full page →nerandomilast →fda approvals ↗
    ›Oct 7, 2025approval311d agoISOTRETINOIN — FDA approvalSun Pharmaceutical Industries Ltd

    Sponsor: AMNEAL PHARMS NY. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Oct 7, 2025approval311d agoSIMPONI (GOLIMUMAB) — FDA approvalJanssen Biotech Inc

    Sponsor: CENTOCOR ORTHO BIOTECH INC. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Oct 7, 2025approval311d agoVEKLURY (REMDESIVIR) — FDA approvalremdesivir

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

    full page →remdesivir →fda approvals ↗
    ›Oct 7, 2025approval311d agoEXEMESTANE — FDA approvalEXEMESTANE

    Sponsor: HIKMA. Form: TABLET. Route: ORAL

    full page →EXEMESTANE →fda approvals ↗
    ›Oct 7, 2025approval311d agoMETHYLIN ER (METHYLPHENIDATE HYDROCHLORIDE) — FDA approvalMETHYLIN ER

    Sponsor: SPECGX LLC. Form: TABLET, EXTENDED RELEASE. Route: ORAL

    full page →METHYLIN ER →fda approvals ↗
    ›Oct 7, 2025approval311d agoLAMOTRIGINE — FDA approvalTorrent Pharma Inc

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

    full page →fda approvals ↗
    ›Oct 7, 2025approval311d agoFEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE (FEXOFENADINE HYDROCHLORIDE) — FDA approvalfexofenadine hydrochloride

    Sponsor: L PERRIGO CO. Form: TABLET, EXTENDED RELEASE. Route: ORAL

    full page →fexofenadine hydrochloride →fda approvals ↗
    ›Oct 7, 2025approval311d agoTOPIRAMATE — FDA approvaltopiramate ER

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

    full page →topiramate ER →fda approvals ↗
    ›Oct 7, 2025approval311d agoRIVAROXABAN — FDA approvalJohnson & Johnson Innovative Medicine

    Sponsor: TARO. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Oct 7, 2025approval311d agoLASIX ONYU (FUROSEMIDE) — FDA approvalFurosemide Sun

    Sponsor: SQ INNOVATION. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →Furosemide Sun →fda approvals ↗
    ›Oct 7, 2025device 510k311d agoDamae Medical — deepLive (OSP12 + DMS) (510k cleared)

    Product code: NQQ. Advisory committee: Radiology. Type: Special

    full page →fda device 510k ↗
    ›Oct 7, 2025device 510k311d agoAcotec Scientific Co., Ltd. — Cedar™ Endovenous Radiofrequency Catheter (ERA-C70-US); Cedar™ Endovenous Radiofrequency Catheter (ERA-C30-US); Endovenous Radiofrequency Generator (ERA-G5-US) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 7, 2025device 510k311d agoEminent Spine — Eminent Spine Posterior SI System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 7, 2025device 510k311d agoOlympus Medical Systems Corporation — Disposable Hot Biopsy Forceps (FD-210U); Disposable Hot Biopsy Forceps (FD-230U) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 7, 2025device 510k311d agoProdeon Medical, Inc. — Prodeon Urethral Sheath System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 7, 2025device 510k311d agoOlympus Medical Systems Corporation — Ultrasonic Bipolar Generator (USG-410); Reuseable Cordless Transducer (TD-410); THUNDERBEAT II Shears with Ultrasonic Mode, 5mm, 45cm (TB2-0545FC); THUNDERBEAT II Shears with Ultrasonic Mode, 5mm, 35cm (TB2-0535FC); THUNDERBEAT II Shears with Ultrasonic Mode, 5mm, 25cm (TB2-0525FC); THUNDERBEAT II Shears with Ultrasonic Mode, 5mm, 20cm (TB2-0520FC) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 7, 2025device 510k311d agoXemis Medical Technology (Shenzhen) Co., Ltd. — Ultrasound Therapy Workstation (XMS-UET2) (510k cleared)NewBay Medical Technology Co Ltd

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

    full page →fda device 510k ↗
    ›Oct 7, 2025device 510k311d agoMetamorphosis GmbH — AIAS Cephalon (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 7, 2025device 510k311d agoVarian Medical Systems, Inc. — TrueBeam, TrueBeam STX, Edge and VitalBeam (510k cleared)MERIT MEDICAL SYSTEMS INC

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

    full page →fda device 510k ↗
    ›Oct 7, 2025device 510k311d agoSt. shine Optical Co., Ltd. — Saview SH Optic 38 UV (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens; Saview SH Optic 38 UV toric (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens; Saview SH Optic 38 UV multifocal (Senofilcon A) Visibility Tinted Soft (Hydrophilic) Contact Lens (510k cleared)

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

    full page →fda device 510k ↗
    ← prev
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    $MMSI91.20+0.10%
    $PRGO12.69-1.25%
    $GILD135.87+0.07%
    $TNDM23.440.00%