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calendar

27,004 catalysts · 17,239 approval · 3,880 device 510k · 2,448 grant · 1,398 device recall · 1,179 device pma · 860 recall

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  • approval17,239
  • device 510k3,880
  • grant2,448
  • device recall1,398
  • device pma1,179
  • recall860
therapy area

no tagged catalysts yet

Week of Feb 10, 2025

50
›Feb 10, 2025device 510k570d agoHebei Ruihe Medical Devices Co., Ltd. — Locking Plates and Screws Systems (510k cleared)

Product code: HRS. Advisory committee: Orthopedic. Type: Abbreviated

full page →fda device 510k ↗
›Feb 10, 2025device 510k570d agoPhilips Consumer Lifestyle B.V. — Philips Lumea IPL (510k cleared)

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

full page →fda device 510k ↗
›Feb 10, 2025device 510k570d agoAbbott Ireland — Calcium2 (510k cleared)

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

full page →fda device 510k ↗
›Feb 10, 2025device 510k570d agoChangsha Anxiang Medical Technology Co., Ltd. — OTC TENS & EMS Unit (510k cleared)

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

full page →fda device 510k ↗
›Feb 10, 2025device 510k570d agoBTL Industries, Inc. — BTL-398 (510k cleared)NL INDUSTRIES INC

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

full page →fda device 510k ↗
›Feb 10, 2025device 510k570d agoRaja Trading Company, Inc. — Myolight Microcurrent Handpiece (510k cleared)

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

full page →fda device 510k ↗
›Feb 10, 2025device 510k570d agoPhilips Ultrasound, LLC — Ultrasound Workspace (UWS 6.0) (510k cleared)

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

full page →fda device 510k ↗
›Feb 11, 2025approval569d agoCAMCEVI KIT (LEUPROLIDE MESYLATE) — FDA approvalForesee Pharmaceuticals Co Ltd

Sponsor: ACCORD. Form: EMULSION. Route: SUBCUTANEOUS

full page →fda approvals ↗
›Feb 11, 2025approval569d agoEVRYSDI (RISDIPLAM) — FDA approvalEVRYSDI

Sponsor: GENENTECH INC. Form: TABLET. Route: ORAL

full page →EVRYSDI →fda approvals ↗
›Feb 11, 2025approval569d agoEVRYSDI (RISDIPLAM) — FDA approvalEVRYSDI

Sponsor: GENENTECH INC. Form: FOR SOLUTION. Route: ORAL

full page →EVRYSDI →fda approvals ↗
›Feb 11, 2025approval569d agoHYDROCODONE BITARTRATE AND ACETAMINOPHEN (ACETAMINOPHEN) — FDA approvalIGC Pharma, Inc.

Sponsor: RHODES PHARMS. Form: TABLET. Route: ORAL

full page →fda approvals ↗
›Feb 11, 2025approval569d agoPEPCID COMPLETE (CALCIUM CARBONATE) — FDA approvalKenvue Inc.

Sponsor: KENVUE BRANDS. Form: TABLET, CHEWABLE. Route: ORAL

full page →fda approvals ↗
›Feb 11, 2025device 510k569d agoGE Medical Systems Ultrasound and Primary Care Diagnostics — Vivid iq (510k cleared)

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

full page →fda device 510k ↗
›Feb 11, 2025device 510k569d agoInfinitum Eta, Ltd. — NUVENTUS NV.C™ Surgical Cassette and Tray (510k cleared)

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

full page →fda device 510k ↗
›Feb 11, 2025device 510k569d agoInbella Medical, Inc. — InbellaBody System (510k cleared)

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

full page →fda device 510k ↗
›Feb 11, 2025device 510k569d agoNoris Medical , Ltd. — LONGY Implant and LONGY-N Implant (510k cleared)

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

full page →fda device 510k ↗
›Feb 11, 2025device 510k569d agoRoche Molecular Systems, Inc. — cobas® SARS-CoV-2 Qualitative for use on the cobas® 5800/6800/8800 Systems (510k cleared)

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

full page →fda device 510k ↗
›Feb 11, 2025device 510k569d agoGuangdong Xinyu Electronic and Technology Co., Ltd. — Wrist Blood Pressure Monitor (XY-W01A, XY-W01B) (510k cleared)

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

full page →fda device 510k ↗
›Feb 11, 2025device 510k569d agoSignus Medizintechnik GmbH — CYLOX® ST (510k cleared)

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

full page →fda device 510k ↗
›Feb 11, 2025device 510k569d agoTeleflex Incorporated — Rusch Endotracheal Tubes (Reinforced); Rusch Endotracheal Tubes (Safety Clear); Rusch Endotracheal Tubes (Safety Clear Pediatric) (510k cleared)TELEFLEX INC

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

full page →fda device 510k ↗
›Feb 11, 2025device 510k569d agoAbbott Diagnostics Scarborough, Inc. — BinaxNOW™ COVID-19 Antigen Self Test (510k cleared)

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

full page →fda device 510k ↗
›Feb 11, 2025device 510k569d agoGE Medical Systems Ultrasound and Primary Care Diagnostics — Vivid T9/Vivid T8 (510k cleared)

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

full page →fda device 510k ↗
›Feb 11, 2025device 510k569d agoMorari, Inc. — MOR (510k cleared)

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

full page →fda device 510k ↗
›Feb 11, 2025device 510k569d agoDongguan Zsr Biomedical Technology Company Limited — Single-Use Digital Flexible Ureteroscope(F-URS) (ZSR-URS-01, ZSR-URS-02, ZSR-URS-03, ZSR-URS-04) (510k cleared)

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

full page →fda device 510k ↗
›Feb 11, 2025device 510k569d agoShoulder Innovations, Inc. — InSet Total Shoulder System (510k cleared)SHOULDER INNOVATIONS, INC.

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

full page →fda device 510k ↗
›Feb 12, 2025approval568d agoMETHYLPREDNISOLONE ACETATE — FDA approvalMETHYLPREDNISOLONE ACETATE

Sponsor: SANDOZ. Form: INJECTABLE. Route: INJECTION

full page →METHYLPREDNISOLONE ACETATE →fda approvals ↗
›Feb 12, 2025approval568d agoMETHYLPREDNISOLONE ACETATE — FDA approvalMETHYLPREDNISOLONE ACETATE

Sponsor: SANDOZ. Form: INJECTABLE. Route: INJECTION

full page →METHYLPREDNISOLONE ACETATE →fda approvals ↗
›Feb 12, 2025approval568d agoIZERVAY (AVACINCAPTAD PEGOL SODIUM) — FDA approvalavacincaptad pegol sodium

Sponsor: ASTELLAS. Form: SOLUTION. Route: INTRAVITREAL

full page →avacincaptad pegol sodium →fda approvals ↗
›Feb 12, 2025approval568d agoPAXLOVID (COPACKAGED) (NIRMATRELVIR) — FDA approvalPAXLOVID (COPACKAGED)

Sponsor: PFIZER. Form: TABLET. Route: ORAL

full page →PAXLOVID (COPACKAGED) →fda approvals ↗
›Feb 12, 2025approval568d agoSELARSDI (USTEKINUMAB-AEKN) — FDA approvalAlvotech

Sponsor: ALVOTECH USA INC. Form: INJECTABLE. Route: INJECTION

full page →fda approvals ↗
›Feb 12, 2025approval568d agoVICTOZA (LIRAGLUTIDE) — FDA approvalSaxenda

Sponsor: NOVO NORDISK INC. Form: SOLUTION. Route: SUBCUTANEOUS

full page →Saxenda →fda approvals ↗
›Feb 12, 2025approval568d agoACETYLCYSTEINE — FDA approvalACETYLCYSTEINE

Sponsor: SOMERSET THERAPS LLC. Form: SOLUTION. Route: INHALATION, ORAL

full page →ACETYLCYSTEINE →fda approvals ↗
›Feb 12, 2025recall568d agoRemedyRepack Inc. recall (Cls II)RemedyRepack Inc

Carvedilol 25 mg Tablet, QTY: 30 Tablets per Blister Pack (3 x 10 blister cards), Rx Only, MFG by: Glenmark, Mahwah, NJ 07430, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC: 70518-3945-00. — Reason: CGMP deviations: presence of N-Nitroso Carvedilol Impurity-1 (NNC 1), above the FDA recommended acceptable intake limit. — Status: Terminated

full page →fda recalls ↗
›Feb 12, 2025recall568d agoPAI Holdings, LLC. dba Pharmaceutical Associates Inc recall (Cls III)Cosette Pharmaceuticals Inc

Guaifenesin and Codeine Phosphate Oral Solution USP, 100mg/10 mg per 5 mL, 16 fl oz (473 ml) bottles, PAI Pharmaceutical Associates, Inc., Greenville, SC 29605, NDC 0121-0775-16 — Reason: Superpotent; sodium benzoate preservative — Status: Completed

full page →fda recalls ↗
›Feb 12, 2025recall568d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

Carvedilol Tablets, USP, 12.5 mg, Rx only, a)500 Tablets, NDC 68462-164-05; b) 100 Tablets, NDC 68462-164-01, Manufactured for Glenmark Pharmaceuticals, NJ. — Reason: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be failing per current FDA recommended limit. — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall568d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

Carvedilol Tablets, USP, 25 mg, Rx only, a)500 Tablets, NDC 68462-165-05; b) 100 Tablets, NDC 68462-165-01, Manufactured for Glenmark Pharmaceuticals, NJ. — Reason: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be failing per current FDA recommended limit. — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall568d agoThe Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recall (Cls II)Aurobindo Pharma USA Inc

Potassium Chloride Extended-Release Tablets, USP, 10 mEq (750 mg), 100 Tablets per carton (10 x 10 unit dose blisters), Rx Only, Distributed by: Aurobindo Pharma USA< INC., 279 Princeton-Hightstown Road, East Windsor, NJ 08520. Made in India. Distributed by: MAJOR PHARMACEUTICALS, Livonia, MI 48152. NDC: 0904-7216-61 — Reason: Failed Dissolution Specifications. — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall568d agoTeva Pharmaceuticals USA, Inc recall (Cls II)Terns Pharmaceuticals, Inc.

Granix (tbo-filgrastim) Injection 300 mcg/0.5 mL, Single Dose prefilled syringe, packaged as a) 1 syringe in 1 CARTON, NDC 63459-910-11, Blister NDC 63459-910-12; (b)10 syringes in 1 CARTON, NDC 63459-910-15, Blister NDC 63459-910-12; (c) 1 syringe in 1 CARTON, NDC 63459-910-17 without safety guard and blister, Rx Only, Manufactured by: UAB Teva Baltics, Vilnius, Lithuania. Distributed by Teva Pharmaceuticals USA, Inc. North Wales PA 19454. Product of Israel. — Reason: Failed Stability Specifications - 12-month stability test result for one of the known peptides is below the specification limit — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall568d agoENDO USA, Inc. recall (Cls I)Par Pharmaceutical Inc

Adrenalin Chloride Solution (Epinephrine Nasal Solution, USP), 30mg/30mL (1mg/mL), packaged in 30 mL vials, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 42023-103-01 — Reason: Labeling: Not Elsewhere Classified: misleading label similar in appearance to the FDA-approved drug product Adrenalin¿ (epinephrine injection, USP) — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall568d agoSKY PACKAGING recall (Cls II)Strides Pharma Science Ltd

HydrALAZINE Hydrochloride, 100 Tablets (10x10), USP, 50mg, Rx only, Manufactured by Strides Pharma Science Ltd, Bengaluru, India, Distributed by McKesson by: McKesson Corporation dba SKY Packaging, TN 38141. NDC 63739-328-10 — Reason: Failed Impurities/Degradation Specifications — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall568d agoSKY PACKAGING recall (Cls II)Strides Pharma Science Ltd

HydrALAZINE Hydrochloride, 25 mg, 100 Unit Dose Tablets (10x10), USP, Rx only, Manufactured by Strides Pharma Science Ltd, Bengaluru, India, Distributed by McKesson by: McKesson Corporation dba SKY Packaging, TN 38141. NDC 63739-327-10 — Reason: Failed Impurities/Degradation Specifications — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall568d agoFDC Limited recall (Cls II)FDC Ltd

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, NDC 64980-514-05. — Reason: Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle. — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025device 510k568d agoKunshan Hi-Fortune Health Products Co., Ltd. — Electrically Powered Wheelchair (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k568d agoAspen Imaging Healthcare, Inc. — AspenView (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k568d agoKunshan Hi-Fortune Health Products Co., Ltd. — Electrically Powered Wheelchair (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k568d agoOpsens, Inc. — OptoMonitor 3 (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k568d agoSiemens Medical Solutions USA, Inc. — NAEOTOM Alpha.Peak/ NAEOTOM Alpha; NAEOTOM Alpha.Pro; NAEOTOM Alpha.Prime (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k568d agoSamsung Medison Co., Ltd. — V8 Diagnostic Ultrasound System; cV8 Diagnostic Ultrasound System; V7 Diagnostic Ultrasound System; cV7 Diagnostic Ultrasound System; V6 Diagnostic Ultrasound System; cV6 Diagnostic Ultrasound System (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k568d agoGi Bionics, LLC — Fecobionics Anorectal System (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k568d agoSubtle Medical, Inc. — SubtleHD (1.x) (510k cleared)

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

full page →fda device 510k ↗
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