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calendar

30,960 catalysts · 18,404 approval · 4,543 device 510k · 3,375 grant · 1,911 device recall · 1,722 device pma · 1,005 recall

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  • approval18,404
  • device 510k4,543
  • grant3,375
  • device recall1,911
  • device pma1,722
  • recall1,005
  • earnings3
therapy area

no tagged catalysts yet

Week of Dec 16, 2024

50
›Dec 18, 2024recall624d agoViatris Inc recall (Cls II)Viatris Inc

Levothyroxine Sodium Tablets USP, 175 mcg, packaged in a) 90-count bottles (NDC 0378-1817-77) and b) 1000-count bottles (NDC 0378-1817-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

full page →fda recalls ↗
›Dec 18, 2024recall624d agoViatris Inc recall (Cls II)Viatris Inc

Levothyroxine Sodium Tablets USP, 137 mcg, packaged in a) 90-count bottles (NDC 0378-1823-77) and b) 1000-count bottles (NDC 0378-1823-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

full page →fda recalls ↗
›Dec 18, 2024recall624d agoViatris Inc recall (Cls II)Viatris Inc

Levothyroxine Sodium Tablets USP, 88 mcg, packaged in a) 90-count bottles (NDC 0378-1807-77) and b) 1000-count bottles (NDC 0378-1807-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

full page →fda recalls ↗
›Dec 18, 2024recall624d agoBiocompatibles UK, Ltd. recall (Cls III)BTG International Inc

Varithena (polidocanol injectable foam) Administration Pack, Contains: 3 silicone-free syringes, 2 compression pads, 1 Varithena Transfer Unit, 1 manometer tubing, Rx Only, Distributed by Biocompatibles Inc., a BTG International Group company. CN01114.3 — Reason: Defective Delivery System: incorrect silicone oil-free NormJect 10 mL Luer Lock Solo syringes packaged in the pack, instead of the required silicone oil-free NormJect 10 mL Luer Solo syringes (luer slip connection). — Status: Terminated

full page →fda recalls ↗
›Dec 18, 2024recall624d agoMckesson Medical-Surgical Inc. Corporate Office recall (Cls II)Antares Pharma Inc

Hylenex recombinant (hyaluronidase) injection, 150 USP units/mL, 4x1 mL Single Dose Vials, Rx only, Manufactured for and marketed by Halozyme, Inc., 12390 El Camino Real San Diego California 92130, Distributed by Antares Pharma, Inc., Ewing, NJ NDC 18657-117-04 — Reason: cGMP Deviations: Temperature excursion — Status: Terminated

full page →fda recalls ↗
›Dec 18, 2024recall624d agoFDC Limited recall (Cls II)FDC Ltd

Timolol Maleate Ophthalmic Solution USP, 0.25%, Sterile, 15mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, NDC 64980-513-15. — 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 ↗
›Dec 18, 2024recall624d agoViatris Inc recall (Cls II)Viatris Inc

Levothyroxine Sodium Tablets USP, 75 mcg, packaged in a) 90-count bottles (NDC 0378-1805-77) and b) 1000-count bottles (NDC 0378-1805-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

full page →fda recalls ↗
›Dec 18, 2024recall624d agoViatris Inc recall (Cls II)Viatris Inc

Levothyroxine Sodium Tablets USP, 25 mcg, packaged in a) 90-count bottles (NDC 0378-1800-77) and b) 1000-count bottles (NDC 0378-1800-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. — Reason: Superpotent Drug and Subpotent Drug: potency failures obtained — Status: Ongoing

full page →fda recalls ↗
›Dec 18, 2024device 510k624d agoCepheid® — Xpert MRSA/SA SSTI (510k cleared)

Product code: NQX. Advisory committee: Microbiology. Type: Special

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoLima Corporate S.P.A. — Physica Porous Femoral Components (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoArtsmedia Denmark Aps — ARTSMedia Semen Wash Medium (510k cleared)

Product code: MQL. Advisory committee: Obstetrics/Gynecology. Type: Traditional

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoArtsmedia Denmark Aps — ARTSMedia Oocyte Aspiration Medium (502020, 502050, 502100) (510k cleared)

Product code: MQL. Advisory committee: Obstetrics/Gynecology. Type: Traditional

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoNatec Medical , Ltd. — Amethyst HP PTA OTW 0.035 Catheter (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoSOADCO, S.L. — Klockner Kits (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoChongqing Moffy Innovation Technology Co., Ltd. — Respiratory Muscle Trainer (510k cleared)Hang Feng Technology Innovation Co., Ltd.

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoViasonix , Ltd. — Falcon/Xpress (Falcon/Xpress) (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoCadwell Industries, Inc. — Bluebird Single-Use Respiratory Effort Belt (510k cleared)POWELL INDUSTRIES INC

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoChangsha Anxiang Medical Technology Co., Ltd. — Tens & Ems Device (TU1080) (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoDeltamed GmbH — 3Delta UNlimited (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoTeknimed Sas — GENTAFIX® (1, 3, 3MV) (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoHunan Vathin Medical Instrument Co., Ltd. — Single-use Flexible Cystoscope (CY-E2E01, CY-E2E01R, CY-E2F01, CY-E2F01R, CY-E2G01, CY-E2G01R, CY-S2E01, CY-S2E01R); Digital Video Monitor (DVM-D1, DVM-D2) (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoVentris Medical — Porous Biologic Scaffold (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoCaerus Corporation — Active System; Avenue8 (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoQuest Medical, Inc. — Lyka® PORT Needle Free Access Device (4170Y) (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoEtex Corporation — EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone ) (510k cleared)

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

full page →fda device 510k ↗
›Dec 18, 2024device 510k624d agoFreudenberg Medical, LLC — FirstFit Surgical Kit (510k cleared)

Product code: EWL. Advisory committee: Ear, Nose, Throat. Type: Traditional

full page →fda device 510k ↗
›Dec 19, 2024approval623d agoGABAPENTIN — FDA approvalGABAPENTIN

Sponsor: STRIDES PHARMA. Form: CAPSULE. Route: ORAL

full page →GABAPENTIN →fda approvals ↗
›Dec 19, 2024approval623d agoGABAPENTIN — FDA approvalGABAPENTIN

Sponsor: STRIDES PHARMA. Form: CAPSULE. Route: ORAL

full page →GABAPENTIN →fda approvals ↗
›Dec 19, 2024approval623d agoGABAPENTIN — FDA approvalGABAPENTIN

Sponsor: STRIDES PHARMA. Form: CAPSULE. Route: ORAL

full page →GABAPENTIN →fda approvals ↗
›Dec 19, 2024approval623d agoGABAPENTIN — FDA approvalAlmatica Pharma LLC

Sponsor: ALKEM. Form: CAPSULE. Route: ORAL

full page →fda approvals ↗
›Dec 19, 2024approval623d agoCEREZYME (IMIGLUCERASE) — FDA approvalimiglucerase

Sponsor: GENZYME. Form: INJECTABLE. Route: INJECTION

full page →imiglucerase →fda approvals ↗
›Dec 19, 2024approval623d agoGABAPENTIN — FDA approvalGABAPENTIN

Sponsor: SANDOZ. Form: CAPSULE. Route: ORAL

full page →GABAPENTIN →fda approvals ↗
›Dec 19, 2024approval623d agoVEKLURY (REMDESIVIR) — FDA approvalremdesivir

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

full page →remdesivir →fda approvals ↗
›Dec 19, 2024device 510k623d agoCardinalhealth — Monoject™ Enteral Syringe with ENFit Connector (401SE); Monoject™ Enteral Syringe with ENFit Connector (403SE); Monoject™ Enteral Syringe with ENFit Connector (406SE); Monoject™ Enteral Syringe with ENFit Connector (412SE); Monoject™ Enteral Syringe with ENFit Connector (435SE); Monoject™ Enteral Syringe with ENFit Connector (460SE) (510k cleared)CARDINAL HEALTH INC

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoWassenburg Medical, Inc. — System 83 Revolve Endoscope Washer/Disinfector (510k cleared)

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoVygon USA — Nutrifit (510k cleared)

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoYongkang Hengyi Vehicle Co., Ltd. — Electric Wheelchair (HC820N) (510k cleared)

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoStryker Neurovascular — Broadway 8 Catheter (510k cleared)

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoJoytech Healthcare Co. , Ltd. — Electric Breast Pump (LD-208L, LD-3010L, LD-2010L, LD-3010, LD-2010) (510k cleared)NVP Healthcare Co Ltd

Product code: HGX. Advisory committee: Obstetrics/Gynecology. Type: Traditional

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoOrthofix Srl — OrthoNext Platform System (510k cleared)

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoInnocare Optoelectronics Corp. — Yushan X-Ray Flat Panel Detector (510k cleared)

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoCollagen Matrix, Inc. — Bovine Dermis Collagen Dermal Matrix (510k cleared)

Product code: KGN. Advisory committee: Unknown. Type: Traditional

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoCristaline Aligners GmbH — Cristaline Aligners Z FLX (510k cleared)

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoDeepHealth, Inc. — Saige-Density (2.5.0) (510k cleared)

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoMedline Industries, LP — Medline Microdissection Needle (4cm) (140936 (ESE104A)); Medline Microdissection Needle (3cm) (140937 (ESE103A)) (510k cleared)

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoBecton, Dickinson and Company — BD Vaginal Panel (510k cleared)BECTON DICKINSON & CO

Product code: PQA. Advisory committee: Microbiology. Type: Special

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoDeepHealth, Inc. — Saige-Dx (3.1.0) (510k cleared)

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoQuickdent Devices Private , Ltd. — Quickdent Dental Implant System (510k cleared)

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoShanghai Sigma High-Tech Co., Ltd. — UV Phototherapy Device (Group A: SQ308PCHFD, SQ308PCQFD, SQ308PCPFD, SQ308PCNFD, SQ308PCMFD); UV Phototherapy Device (Group B: SQ308PHTFF, SQ308PHSFF, SQ308PHRFF, SQ308PHZFG, SQ308PPUFF, SQ308PPVFF, SQ308PPWFG) (510k cleared)

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

full page →fda device 510k ↗
›Dec 19, 2024device 510k623d agoSynchrony Medical , Ltd. — LibAirty Airway Clearance System (510k cleared)

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

full page →fda device 510k ↗
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$VTRS16.63+0.73%
$FOFO3.0000+2.39%
$VTRS16.63+0.73%
$POWL
$VTRS16.63+0.73%
$VTRS16.63+0.73%
$VTRS16.63+0.73%
$GILD149.92+2.45%
$CAH245.49+2.57%
$BDX190.48+1.80%