{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-10-26",
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        "TransOs Tunneler Inner Shaft (component)",
        "VersaTip Suture Passer Tip, Crescent, 5/box",
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        "Complaint File Establishment per 21 CFR 820.198",
        "Repack or Relabel Medical Device",
        "Develop Specifications But Do Not Manufacture At This Facility",
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "3021286087",
        "fei_number": "3021286087",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "TENSOR SURGICAL, INC.",
        "address_line_1": "6345 S Pecos Rd Ste 212",
        "address_line_2": "",
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        "iso_country_code": "US",
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        "us_agent": {},
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          "owner_operator_number": "10083936",
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            "first_name": "Justin",
            "middle_initial": "",
            "last_name": "Anderson",
            "subaccount_company_name": "",
            "phone_number": "1-702-4760771-x"
          },
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            "address_1": "6345 S Pecos Rd Ste 212",
            "address_2": "",
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          "created_date": "2021-12-31",
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            "device_name": "Orthopedic Manual Surgical Instrument",
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}