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© 2026 BizmoonPrivacyTermsCredits
  1. Home
  2. Regulations
  3. Federal
  4. Page 3

Federal regulations

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    Recency
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    FCCRemove filter: FCCFDARemove filter: FDAClear all
    • Medical Devices; Immunology and Microbiology Devices; Classification of the Simple Point-of-Care Device to Directly Detect SARS-CoV-2 Viral Targets From Clinical Specimens in Near-Patient Settings
      June 11, 2026

      FDA classifies simple point-of-care SARS-CoV-2 detection devices as Class II medical devices, requiring special controls to ensure safety and effectiveness while reducing regulatory burden for manufacturers.

    • Azuma Foods International, Inc. Issues Allergy Alert on Undeclared Fish in Tako Wasabi
      June 11, 2026

      Azuma Foods International recalls 545 cases of 3-pack Tako Wasabi seasoned octopus due to undeclared fish allergen that poses serious risk to consumers with fish allergies.

    • Recommendations on Scale-Up and Postapproval Changes Guidances for Industry; Request for Comments; Reopening of the Comment Period
      June 11, 2026

      FDA reopens the comment period for its industry guidance on scale-up and postapproval changes for drug dosage forms to allow additional stakeholder input.

    • Drug Repurposing for Unmet Medical Needs; Request for Information; Extension of Comment Period
      June 11, 2026

      FDA extends the comment period for its drug repurposing request for information to allow stakeholders additional time to submit input on addressing unmet medical needs.

    • Amending Over-the-Counter Monograph M020: Sunscreen Drug Products for Over-the-Counter Human Use, and Related Information
      June 10, 2026

      FDA amends sunscreen monograph M020 to add bemotrizinol at concentrations up to 6 percent as a generally recognized as safe and effective active ingredient for over-the-counter sunscreen products.

    • Medical Devices; Ear, Nose, and Throat Devices; Classification of the Combined Acoustic and Electrical External Stimulation Device for the Relief of Tinnitus
      June 10, 2026

      FDA classifies combined acoustic and electrical external stimulation devices for tinnitus relief as Class II medical devices, subject to special controls to ensure safety and effectiveness.

    • Clover Hill Dairy Recalls Soft Ricotta/Requeson Cheese Due to Possible Health Risk
      June 9, 2026

      Clover Hill Dairy voluntarily recalls all Soft Ricotta/Requeson Cheese products due to potential Listeria monocytogenes contamination posing health risks to vulnerable populations.

    • GO Raw LLC. Expands Voluntary Recall to Include One Lot of Steve’s Real Food Freeze-Dried Chicken Recipe Due to Low Thiamine (Vitamin B1) Levels
      June 8, 2026

      GO Raw LLC expands its February 17, 2026 recall of Steve's Real Food Freeze-Dried Chicken Recipe to include an additional lot due to potentially low thiamine (Vitamin B1) levels.

    • Information Collections Being Submitted for Review and Approval to Office of Management and Budget
      June 8, 2026

      FCC seeks public comment on information collection burdens and specifically invites small businesses with fewer than 25 employees to suggest paperwork reduction measures under the Small Business Paperwork Relief Act of 2002.

    • Information Collection Being Reviewed by the Federal Communications Commission
      June 8, 2026

      The Federal Communications Commission invites public comment on information collection requirements under the Paperwork Reduction Act, with specific focus on reducing burdens for small businesses with fewer than 25 employees.

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