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17,794 catalysts · 4,728 grant · 3,126 8k filing · 2,606 approval · 2,051 device 510k · 1,649 device recall · 1,418 device pma

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  • grant4,728
  • 8k filing3,126
  • approval2,606
  • device 510k2,051
  • device recall1,649
  • device pma1,418
device adverse event
1,000
  • earnings583
  • recall551
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
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    • Immunology35
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    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Sep 1, 2025

    50
    ›Sep 2, 2025device 510k344d agoChengdu Besmile Medical Technology Co., Ltd. — Customized Abutment and Screw (510k cleared)

    Product code: NHA. Advisory committee: Dental. Type: Abbreviated

    full page →fda device 510k ↗
    ›Sep 2, 2025device 510k344d agoAerogen, Ltd. — Aerogen Pro-X1 Controller System (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 2, 2025device 510k344d agoPhilips Medizin Systeme Böblingen GmbH — IntelliVue Patient Monitor 6100 (6100); IntelliVue Patient Monitor 6300 (6300); IntelliVue Patient Monitor 6500 (6500) (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 2, 2025device 510k344d agoNaitive Technologies, Ltd. — OsteoSight™ Hip (v1) (510k cleared)TAT TECHNOLOGIES LTD

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

    full page →fda device 510k ↗
    ›Sep 2, 2025device 510k344d agoVelmeni, Inc. — VELMENI for DENTISTS (V4D) (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 2, 2025device 510k344d agoIgnite Orthomotion — Achieve Partial Knee System - Porous Coated CoCrMo Femoral Component (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 2, 2025device pma344d agoBoston Scientific Corp — Opal HDx Ablation Connection Box (Maestro); Opal HDx Ablation Connection Box - IntellaNav StablePoint; Opal HDx Ablation (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: Normal 180 Day Track No User Fee. Product code: OAD. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Sep 2, 2025device pma344d agoJohnson & Johnson Surgical Vision, Inc. — TECNIS™ Toric II 1-Piece IOLs, ZCU TECNIS Symfony Toric II Extended Range of Vision IOLs, ZXU TECNIS Eyhance Toric II IO (PMA supplement)JOHNSON & JOHNSON

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

    full page →fda device pma ↗
    ›Sep 2, 2025device pma344d agoCochlear Americas — Cochlear™ Nucleus® System (PMA supplement)

    Supplement type: Normal 180 Day Track No User Fee. Product code: MCM. Advisory committee: EN. Decision: APPR

    full page →fda device pma ↗
    ›Sep 2, 2025device pma344d agoJohnson & Johnson Surgical Vision, Inc. — TECNIS 3-Piece Acrylic Monofocal, Model ZA9003 (PMA supplement)JOHNSON & JOHNSON

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

    full page →fda device pma ↗
    ›Sep 2, 2025device pma344d agoCentinel Spine, LLC — PRODISC L (PMA supplement)

    Supplement type: Normal 180 Day Track No User Fee. Product code: MJO. Advisory committee: OR. Decision: APPR

    full page →fda device pma ↗
    ›Sep 2, 2025device pma344d agoRxsight, Inc. — LIGHT ADJUSTABLE LENS (LAL) AND LIGHT DELIVERY DEVICE (LDD) (PMA supplement)RxSight, Inc.

    Supplement type: Normal 180 Day Track No User Fee. Product code: PZK. Advisory committee: OP. Decision: APPR

    full page →fda device pma ↗
    ›Sep 2, 2025device pma344d agoJohnson & Johnson Surgical Vision, Inc. — TECNIS 3-Piece Multifocal, Model ZMA00 (PMA supplement)JOHNSON & JOHNSON

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

    full page →fda device pma ↗
    ›Sep 2, 2025device pma344d agoHeartsine Technologies, Ltd. — HeartSine’s samaritan® Public Access Automated External Defibrillators (SAM 350P, SAM 360P and SAM 450P) and Accessories (PMA supplement)TAT TECHNOLOGIES LTD

    Supplement type: Special (Immediate Track). Product code: MKJ. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Sep 2, 2025device recall344d agoCanon Medical System, USA, INC. device recall (Cls II)

    This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen and lower extremities. — Reason: It has been found that when SPOT Fluoro is first turned on, the default ROI is selected and the collimator blades move to the boundary of the ROI, and the static image is overlayed around the ROI, covering the collimated area. If the customer changes the ROI, the collimator blades and static images are adjusted accordingly. However, when the acquisition program is changed, the collimator returns to the default ROI position which may be larger than the specified one, leaving the X-ray area partially covered by the static image. This is a software problem with the SPOT Fluoro program and will not occur if the function is not used. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 2, 2025device recall344d agoLeMaitre Vascular, Inc. device recall (Cls II)LEMAITRE VASCULAR INC

    Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616, (2) AG 630, (3) AG 636, (4) AG 640, (5) AG 645, (6) AG 715, (7) AG 730, (8) AG 735, (9) AG 740, (10) AG 745, (11) AG 750, (12) AG 830, (13) AG 840, (14) AG 1015, (15) AG 1030; — Reason: The bovine carotid arteries used to produce the impacted grafts from affected lots were sourced using raw material from a supplier that had not been reviewed and approved by the appropriate regulatory authority. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 2, 2025device recall344d agoBerkeley Advanced Biomaterials, LLC device recall (Cls II)

    Tribio Implant 7.5mm x 40mm REF M80 SB008 UDI code: (01) 00816125023653(10) EBL10B13C(17) 270630 Tribio" Implant is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. — Reason: Due to incorrect product label (Incorrect product name identified on outer packaging). — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 3, 2025approval343d agoSKYRIZI (RISANKIZUMAB-RZAA) — FDA approvalrisankizumab

    Sponsor: ABBVIE INC. Form: INJECTABLE. Route: INTRAVENOUS

    full page →risankizumab →fda approvals ↗
    ›Sep 3, 2025approval343d agoSKYRIZI (RISANKIZUMAB-RZAA) — FDA approvalrisankizumab

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

    full page →risankizumab →fda approvals ↗
    ›Sep 3, 2025approval343d agoVIGAFYDE (VIGABATRIN) — FDA approvalPyros Pharmaceuticals Inc.

    Sponsor: PYROS PHARMS. Form: SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Sep 3, 2025approval343d agoVIGAFYDE (VIGABATRIN) — FDA approvalPyros Pharmaceuticals Inc.

    Sponsor: PYROS PHARMS. Form: SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Sep 3, 2025approval343d agoTRAMADOL HYDROCHLORIDE — FDA approvaltramadol hydrochloride ER

    Sponsor: RUBICON RESEARCH. Form: TABLET. Route: ORAL

    full page →tramadol hydrochloride ER →fda approvals ↗
    ›Sep 3, 2025approval343d agoRYBREVANT (AMIVANTAMAB-VMJW) — FDA approvalamivantamab

    Sponsor: JANSSEN BIOTECH. Form: INJECTABLE. Route: INJECTION

    full page →amivantamab →fda approvals ↗
    ›Sep 3, 2025recall343d agoMEDLINE INDUSTRIES, LP - Northfield recall (Cls II)

    Good Neighbor Pharmacy, Alcohol Prep Pads, Distributed By AmeriSource Bergen, 1 West First Avenue, Conshohocken, PA 19428, Made in China: 100 eaches per box, 30 boxes per case, (3,000 eaches per case), NDC 46122-043-78. — Reason: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. — Status: Ongoing

    full page →fda recalls ↗
    ›Sep 3, 2025recall343d agoMEDLINE INDUSTRIES, LP - Northfield recall (Cls II)

    CURAD Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per Carton, 30 Boxes per Case, Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093, USA, Made in India, www.curad.com, 1-800-633-5463, NDC 53329-827-30 — Reason: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. — Status: Ongoing

    full page →fda recalls ↗
    ›Sep 3, 2025recall343d agoCardinal Health Inc. recall (Cls II)CARDINAL HEALTH INC

    Enoxaparin Sodium Injection, USP, 30 mg/0.3 mL, packaged in 0.3 mL prefilled syringes further packaged in bags of 5 prefilled syringes, Rx Only, Dist. by: Sandoz Inc., Princeton, NJ 08540, Outer package - NDC 55154-3543-5, Inner label - NDC 0781-3238-01 — Reason: Correct Labeled Product Mispack: Bags labeled for Enoxaparin Sodium Injection, 80 mg/0.8 mL, contained Enoxaparin Sodium Injection, 30 mg/0.3 mL — Status: Ongoing

    full page →fda recalls ↗
    ›Sep 3, 2025recall343d agoMEDLINE INDUSTRIES, LP - Northfield recall (Cls II)

    ReliOn, Sterile Alcohol Swabs, Skin Cleanser, 200 Swabs, Distributed by, Walmart, Inc., Bentonville, AR 72716 Walmart: 200 eaches per box, 24 boxes per case (4,800 eaches per case), NDC 49035-814-60. — Reason: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. — Status: Ongoing

    full page →fda recalls ↗
    ›Sep 3, 2025recall343d agoBaxter Healthcare Corporation recall (Cls II)Baxter Healthcare Corp

    Acetaminophen Injection 1000 mg/100 mL (10 mg/mL), packaged in 100 mL Viaflo container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Made in Ireland, NDC 36000-306-60. — Reason: Discoloration — Status: Ongoing

    full page →fda recalls ↗
    ›Sep 3, 2025recall343d agoMEDLINE INDUSTRIES, LP - Northfield recall (Cls II)

    Medline Alcohol Prep Pads, 70% Isopropyl Alcohol, 100 Sterile 2-Ply Pads, Single Use Only, Large, www.medline.com, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093 USA, 1-800-MEDLINE, NDC 53329-811-30. — Reason: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. — Status: Ongoing

    full page →fda recalls ↗
    ›Sep 3, 2025recall343d agoLannett Company Inc. recall (Cls II)Lannett Co Inc

    Lisdexamfetamine Dimesylate Capsules, 40 mg, 100-count bottles, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC 0527-4664-37 — Reason: Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate Capsules 40mg, contained Lisdexamphetamine Dimesylate Capsules 30mg. — Status: Completed

    full page →fda recalls ↗
    ›Sep 3, 2025recall343d agoAmerisource Health Services LLC recall (Cls II)AltrixBio Inc

    Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217 NDC 60687-695-01 - Carton NDC [60687-695-11- Unit Dose] — Reason: CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated. — Status: Ongoing

    full page →fda recalls ↗
    ›Sep 3, 2025recall343d agoMEDLINE INDUSTRIES, LP - Northfield recall (Cls II)

    RITE AID PHARMACY, first aid alcohol prep pads, DISTRIBUTED BY: RITE AID. 200 NEWBERRY COMMONS, ETTERS, PA 17319, NDC 11822-5156-2. — Reason: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. — Status: Ongoing

    full page →fda recalls ↗
    ›Sep 3, 2025recall343d agoMEDLINE INDUSTRIES, LP - Northfield recall (Cls II)

    H-E-B, inControl, Sterile* Alcohol Pads, CONT. 100 PADS, Packaged in China with components from Taiwan, Elaborado Con Orgullo Y Cuidado PARA H-E-B, San Antonio, TX 78204, NDC 37808-809-09. — Reason: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration. — Status: Ongoing

    full page →fda recalls ↗
    ›Sep 3, 2025device 510k343d agoAlphatec Spine — IdentiTi™ II ALIF Standalone Interbody System; Transcend™ ALIF Standalone Interbody System (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 3, 2025device 510k343d agoRestor3D — Kinos Total Ankle System (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 3, 2025device 510k343d agoMedicreations, LLC — MEDILIGHT (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 3, 2025device 510k343d agoForest Devices, Inc. — SignalNED System (Model RE) (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 3, 2025device 510k343d agoA-1 Engineering — NeurotriS (SX2500); NeurotriS (SX3800) (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 3, 2025device 510k343d agoAvita Corporation — AViTA Arm Type Blood Pressure Monitor Cuff (510k cleared)Teva Pharmaceuticals USA Inc

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

    full page →fda device 510k ↗
    ›Sep 3, 2025device 510k343d agoDongguan E-Test Technology Co., Ltd. — Automatic Upper Arm Blood Pressure Monitor (BA-831X, BA-832X, BA-833X, BA-837X, BA-838X, BA-842X, BA-843X, BA-845X, BA-847X, BA-849X, BA-851X, BA-852X, BA-855X, BA-835, BA-836, BA-839, BA-840, BA-856) (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 3, 2025device 510k343d agoBlessing Cathay Corporation — AquaCast Mask (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 3, 2025device 510k343d agoBeijing Superlaser Technology Co., Ltd. — Diode laser therapy device (VADER) (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 3, 2025device 510k343d agoAgnes Medical Co., Ltd. — AGNES Ultra (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 3, 2025device 510k343d agoArterys, Inc. — Tempus Pixel (510k cleared)Arteris, Inc.

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

    full page →fda device 510k ↗
    ›Sep 3, 2025device 510k343d agoPrismatik Dentalcraft, Inc. — BruxZir® NOW (510k cleared)

    Product code: EIH. Advisory committee: Dental. Type: Special

    full page →fda device 510k ↗
    ›Sep 3, 2025device pma343d agoSymatese — EVOLYSSE® FORM and EVOLYSSE® SMOOTH (PMA supplement)

    Supplement type: Normal 180 Day Track No User Fee. Product code: LMH. Advisory committee: SU. Decision: APPR

    full page →fda device pma ↗
    ›Sep 3, 2025device pma343d agoBolton Medical, Inc. — RelayPro (PMA supplement)

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

    full page →fda device pma ↗
    ›Sep 3, 2025device pma343d agoMicroTransponder, Inc. — Vivistim® System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: QPY. Advisory committee: PM. Decision: OK30

    full page →fda device pma ↗
    ›Sep 3, 2025device pma343d agoSirtex Medical, Inc. — Lava Liquid Embolic System (Lava LES) and Lava Mixing Kit (PMA supplement)

    Supplement type: Normal 180 Day Track No User Fee. Product code: QVG. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Sep 3, 2025device pma343d agoBoston Scientific Corp — ACUITY X4 Straight, Models 4671 and 4672; ACUITY X4 Spiral S, Models 4674 and 4675; ACUITY X4 Spiral L, Models 4677 and (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: Real-Time Process. Product code: NIK. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
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