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calendar

22,394 catalysts · 4,728 grant · 4,392 device 510k · 3,350 8k filing · 3,181 approval · 2,000 device pma · 2,000 device recall

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2026-08-10: 0 catalysts2026-08-11: 0 catalysts2026-08-12: 0 catalysts2026-08-13: 0 catalysts2026-08-14: 66 catalysts2026-08-15: 0 catalysts2026-08-16: 0 catalysts2026-08-17: 1 catalyst2026-08-18: 2 catalysts2026-08-19: 3 catalysts2026-08-20: 0 catalysts2026-08-21: 0 catalysts2026-08-22: 0 catalysts2026-08-23: 0 catalysts2026-08-24: 0 catalysts2026-08-25: 0 catalysts2026-08-26: 1 catalyst2026-08-27: 1 catalyst2026-08-28: 0 catalysts2026-08-29: 0 catalysts2026-08-30: 0 catalysts2026-08-31: 0 catalysts2026-09-01: 1 catalyst2026-09-02: 0 catalysts2026-09-03: 1 catalyst2026-09-04: 0 catalysts2026-09-05: 0 catalysts2026-09-06: 0 catalysts2026-09-07: 0 catalysts2026-09-08: 0 catalysts2026-09-09: 0 catalysts2026-09-10: 0 catalysts2026-09-11: 0 catalysts2026-09-12: 0 catalysts2026-09-13: 0 catalysts2026-09-14: 0 catalysts2026-09-15: 0 catalysts2026-09-16: 0 catalysts2026-09-17: 0 catalysts2026-09-18: 0 catalysts2026-09-19: 0 catalysts2026-09-20: 0 catalysts2026-09-21: 0 catalysts2026-09-22: 0 catalysts2026-09-23: 2 catalysts2026-09-24: 0 catalysts2026-09-25: 0 catalysts2026-09-26: 0 catalysts2026-09-27: 0 catalysts2026-09-28: 0 catalysts2026-09-29: 0 catalysts2026-09-30: 0 catalysts2026-10-01: 0 catalysts2026-10-02: 0 catalysts2026-10-03: 0 catalysts2026-10-04: 0 catalysts2026-10-05: 0 catalysts2026-10-06: 0 catalysts2026-10-07: 0 catalysts2026-10-08: 2 catalysts2026-10-09: 0 catalysts2026-10-10: 0 catalysts2026-10-11: 0 catalysts2026-10-12: 0 catalysts2026-10-13: 1 catalyst2026-10-14: 1 catalyst2026-10-15: 0 catalysts2026-10-16: 0 catalysts2026-10-17: 0 catalysts2026-10-18: 0 catalysts2026-10-19: 1 catalyst2026-10-20: 2 catalysts2026-10-21: 2 catalysts2026-10-22: 2 catalysts2026-10-23: 1 catalyst2026-10-24: 0 catalysts2026-10-25: 0 catalysts2026-10-26: 1 catalyst2026-10-27: 8 catalysts2026-10-28: 12 catalysts2026-10-29: 21 catalysts2026-10-30: 4 catalysts2026-10-31: 0 catalysts2026-11-01: 0 catalysts2026-11-02: 9 catalysts2026-11-03: 18 catalysts2026-11-04: 22 catalysts2026-11-05: 37 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts
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  • grant4,728
  • device 510k4,392
  • 8k filing3,350
  • approval3,181
  • device pma2,000
  • device recall2,000
recall
1,078
  • device adverse event1,000
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Dec 16, 2024

    6
    ›Dec 20, 2024device 510k603d agoHandpiece Headquarters — HPR Cordless Hygiene Handpiece (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 20, 2024device 510k603d agoRizhao Huge Biomaterials Company, Ltd. — TopCEM-Try in Veneer Try-in Gel (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 20, 2024device 510k603d agoSynergy Biomedical — BioSphere Putty; BioSphere MIS Putty (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 21, 2024device 510k602d agoLight Guide Optics International , Ltd. — LGO-Surgical Laser Fibers (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 21, 2024device 510k602d agoZhuzhou Goldenhot Medical Technology Co., Ltd. — IPL Hair Removal Device (DE03A-W, DE03A-P, DE03A-V, DE03A-G, DE03B-W, DE03B-P, DE03B-V, DE03B-G) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 22, 2024device 510k601d agoJiangxi Medex Technology Co., Ltd. — SLT Select Fiber Delivery System and Contact Tips (models: SSRH 8-SMA; TCRH 7-SMA; FEF 2.2-SMA; CFE 0.6-SMA; SSRH 8Z-SMA; SSRH 4-SMA; SSRH 6-SMA; SSRH 9-SMA; SSRH 10-SMA; SSRH 11-SMA; SSRH 7L-SMA; TCRH 7Z-SMA; FEF 1.8-SMA; CFE 0.55-SMA; CFE 0.36-SMA; LAL 550-SMA; LAL 550Z-SMA; LAL 365-SMA; LAL 365Z-SMA; ER2; ERP2; GR2; GRP2; ER4; ERP4; GR4; GRP4; ER6; ERP6; GR6; GRP6; ER8; ERP8; GR8; GRP8; ER10; ERP10; GR10; GRP10; ER12; ERP12; GR12; GRP12; MD2.5; MD3.5; HP1.0; MTP1.5; MTP3.5; MTRG1.5; (510k cleared)Jiangsu Maoxing Technology Co Ltd

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

    full page →fda device 510k ↗

    Week of Dec 23, 2024

    44
    ›Dec 23, 2024approval600d agoYUFLYMA (ADALIMUMAB-AATY) — FDA approvalYUFLYMA

    Sponsor: CELLTRION. Form: INJECTABLE. Route: INJECTION

    full page →YUFLYMA →fda approvals ↗
    ›Dec 23, 2024device 510k
    ← prev
    page 8 of 448
    next →
    600d ago
    Noraker — GlassBone Granules (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoJiangsu Lici Medical Device Co., Ltd. — NIDO Baby Magnetic Resonance Imaging System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoShandong Int Medical Instruments Co., Ltd. — Angiography Injector (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoCanon Medical Systems Corporation — Aquilion ONE (TSX-308A/3) V1.5 (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoRiton 3D Technology Co., Ltd. — Denture Base (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoBeijing Taktvoll Technology Co., Ltd. — Electrosurgical Generator (ES-100); Electrosurgical Generator (ES-300) (510k cleared)Beijing Geekplus Technology Co., Ltd./ADR

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoHlb Lifescience Co., Ltd. — Sofjec (Single use Needle); Sofjec (Single use Syringe with or without Needle); Sofjec (Membrane Filter Syringe) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoInogen, Inc. — SIMEOX 200 Airway Clearance Device (510k cleared)Inogen Inc

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoNrt X-Ray A/S — Adora DRFi (04550010) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoGenadyne Biotechnologies, Inc. — Genadyne DUO NPWT (510k cleared)POP Biotechnologies Inc

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoElastimed , Ltd. — SACS PRO (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoBelmont Medical Technologies — Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 1000 ml/min); Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 750 ml/min) (510k cleared)Medical Care Technologies Inc.

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoSurGenTec, LLC — OsteoFlo HydroFiber (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoPanopticAI technologies Limited — PanopticAI Vital Signs (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoNox Medical Ehf — Noxturnal Web (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoFusion Orthopedics — Bolo Button System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoDepuy Ireland UC — INHANCE INTACT™ (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoArtfx Medical — ARTFX Trauma Bone Plate and Screw System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 23, 2024device 510k600d agoNeo Medical SA — NEO Pedicle Screw System™ (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 24, 2024device 510k599d agoChirana T. Injecta — Insulin Syringes (510k cleared)Shanghai Jiao Tong University

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

    full page →fda device 510k ↗
    ›Dec 24, 2024device 510k599d agoSurgical Theater, Inc. — SpineAR SNAP (SyncAR Spine) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 25, 2024recall598d agoKeystone Industries recall (Cls II)

    Gelato, Benzocaine 20% Topical Gel Anesthetic Gel, Net Wt. 1 oz. (30ml), Manufactured by Keystone Industries 480 S. Democrat Rd., Gibbstown, NJ 08027, NDC# 68400-352-30. — Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. — Status: Completed

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoKeystone Industries recall (Cls II)HENRY SCHEIN INC

    Henry Schein, Benzo-Jel, Topical Anesthetic Gel, 20% Benzocaine, 1 fl. oz. (29.6 mL), Distributed by Henry Schein, Melville, NY 11747, For Professional Use Only, — Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. — Status: Completed

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoKeystone Industries recall (Cls II)MADE IN USA INC.

    Quala Dental Products, Topical Anesthetic Gel, Contains 20% Benzocaine, Net Contents: 1 oz (30g), Gluten Free, Quala Dental Products, Made in USA for: NDC, Inc, 407 New Sanford Road, La Vergne, TN 37086, www.quala.com — Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. — Status: Completed

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoProvepharm Inc. recall (Cls II)Bausch Health US LLC

    Dihydroergotamine Mesylate Injection, solution for injection, USP, 1 mg/mL Ampules, Rx Only, Distributed by: Provepharm Inc. 100 Springhouse Drive Suite 105, Collegeville, PA 19426, NDC 81284-411-05 — Reason: Discoloration — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoKeystone Industries recall (Cls II)MADE IN USA INC.

    safco, SensiCaine Ultra, Topical Anesthetic Gel, Contains 20% Benzocaine, 1 oz (29.6 mL), Cherry, NDC 67239-0219-1, Gluten Free, Distributed by: Safco Dental Supply Co., Buffalo Grove, IL 60089, Made in USA, For Professional Use Only. — Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. — Status: Completed

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoKeystone Industries recall (Cls II)

    Dental City, Topical Anesthetic Gel, Benzocaine 20%, Net Content: 1 oz. (30 ml), Gluten Free, Manufactured for: Dental City, Green Bay, WI 54311, dentalcity.com. — Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. — Status: Completed

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoKeystone Industries recall (Cls II)MADE IN USA INC.

    Health-Tec, Topical Anesthetic Gel, Benzocaine 20%, Made in USA, 1 FL. OZ (29.6 ml), NDC 69634-021-30. — Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. — Status: Completed

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoKeystone Industries recall (Cls II)

    Primo, Topical Anesthetic gel, Benzocaine 20%, Net Content: 1 oz. (30g), Gluten Free, Manufactured for: Primo Dental Products, 845 Third Avenue, 6th Floor, New York, NY 10022. — Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. — Status: Completed

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoRegenerative Processing Plant, LLC recall (Cls II)

    LITE Regener-Eyes, Ophthalmic Solution (glycerin 0.4%), 3mL bottles, Distributed by: Regener-Eyes, Tampa, FL; Manufactured by: Regenerative Processing Plant, LLC, 34176 US HWY 19N, FL, NDC 82305-006-01 — Reason: Lack of Sterility Assurance — Status: Terminated

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoKeystone Industries recall (Cls II)

    Pearson Quality, Topical Anesthetic Gel, 20% Benzocaine, For Professional Use Only, Net Contents: 1 oz (30 g), Manufactured for Pearson Dental Supply Inc., Sylmar, CA 91342 USA. — Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. — Status: Completed

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoApothecus Pharmaceutical Corp. recall (Cls II)NYMOX PHARMACEUTICAL CORP

    VCF, Vaginal Contraceptive Gel, Birth Control, 10 Pre-filled Applicators, Net Wt. 0.09 oz (2.55g) Each, Distributed By: Apothecus Pharmaceutical Corp., Ronkonkoma, NY 11779, NDC 52925-512-10 — Reason: CGMP deviations: out of specifications for assay — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoKeystone Industries recall (Cls II)

    M&S Dental Supply Co LLC., Topical Anesthetic Gel, Benzocaine 20%, Net Wt. 1 oz. (30ml), Manufactured for: M&S Dental Supply Co LL, 105-30 101 Avenue, Ozone Park, NY 11416. — Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. — Status: Completed

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoAurobindo Pharma USA Inc recall (Cls II)Aurobindo Pharma USA Inc

    Nebivolol Tablets, 2.5. mg, 30-count bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, East Windsor, NJ 08520. NDC: 59651-137-30 — Reason: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-Nitroso Nebivolol above acceptable intake (AI) limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoKeystone Industries recall (Cls II)

    Ipana, 20% Benzocaine Topical Gel, 28g, Maxill Inc., St Thomas ON Canada. — Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. — Status: Completed

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoMacleods Pharmaceuticals Ltd recall (Cls II)Telix Pharmaceuticals Ltd

    Olanzapine Tablets, USP 2.5 mg, 30-count bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540, Manufactured for: Macleods Pharma USA Inc. Princeton, NJ,08540: Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi Himachal Pradesh, INDIA, NDC 33342-067-07. — Reason: Failed Impurities/Degradation Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoKeystone Industries recall (Cls II)

    Burkhart, Topical Anesthetic Gel, Benzocaine 20%, Gluten Free, 1 FL. OZ (30 ml), Manufactured for Burkhart Dental Supply, Tacoma, Washington 98409. — Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. — Status: Completed

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoKeystone Industries recall (Cls II)

    Patterson Dental, Patterson Topical Anesthetic Gel, Benzocaiine, 1 oz. (30 ml), Manufactured for (Fabrique pour): Patterson Dental Supply, Inc. 1031 Mendota Heights Road, Saint Paul, MN 55120, NDC 50227-1002-3. — Reason: CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers. — Status: Completed

    full page →fda recalls ↗
    ›Dec 25, 2024recall598d agoRegenerative Processing Plant, LLC recall (Cls II)

    PROFESSIONAL Regener-Eyes, Ophthalmic Solution (glycerin 0.5%) , 3mL bottles, Distributed by: Regener-Eyes, Tampa, FL; Manufactured by: Regenerative Processing Plant, LLC, 34176 US HWY 19N, FL, NDC 82305-003-01 — Reason: Lack of Sterility Assurance — Status: Terminated

    full page →fda recalls ↗
    ›Dec 26, 2024approval597d agoEBANGA (ANSUVIMAB-ZYKL) — FDA approvalansuvimab

    Sponsor: RIDGEBACK BIOTHERAPEUTICS. Form: POWDER. Route: IV (INFUSION)

    full page →ansuvimab →fda approvals ↗
    ›Dec 26, 2024approval597d agoWEZLANA (USTEKINUMAB-AUUB) — FDA approvalWEZLANA

    Sponsor: AMGEN INC. Form: INJECTABLE. Route: INTRAVENOUS, SUBCUTANEOUS

    full page →WEZLANA →fda approvals ↗
    ›Dec 26, 2024approval597d agoWEZLANA (USTEKINUMAB-AUUB) — FDA approvalWEZLANA

    Sponsor: AMGEN INC. Form: INJECTABLE. Route: INTRAVENOUS, SUBCUTANEOUS

    full page →WEZLANA →fda approvals ↗
    ›Dec 26, 2024device 510k597d agoInstitut Straumann AG — Straumann CARES Visual and Nova Dental CAD (510k cleared)

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

    full page →fda device 510k ↗
    $USDW
    $MDCE0.00020.00%
    $INGN
    $AMGN415.21-0.63%
    $TLX
    $BJGPY
    $NYMXF
    $USDW
    $USDW
    $HSIC72.44-2.60%
    $AMGN415.21-0.63%