Teton Fall Detection

GUDID 05745001037000

Teton's Fall Detection system uses a device equipped with a camera to monitor the room, analyzing live video feeds through AI models that are processed locally. These models interpret human activity within the camera’s field of view and make real-time predictions, specifically detecting falls. At night, infrared lighting is used to enhance visibility, ensuring continuous monitoring. Once a fall is detected, the processed data is securely transmitted to care staff through a dedicated server, enabling timely intervention. The focus of this feature is precision and reliability, ensuring patient safety while minimizing system complexity by concentrating solely on fall detection rather than the broader ecosystem of the Teton One system.

Teton.AI ApS

Inpatient motion surveillance software

• Primary Device ID: 05745001037000
• NIH Device Record Key: cee98e3c-7a45-4924-8c68-b76a9b37b8ad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Teton Fall Detection
• Version Model Number: R1.0
• Company DUNS: 306198002
• Company Name: Teton.AI ApS
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05745001037000 [Primary]

FDA Product Code

• PJO: Fall Prevention Alarm/Sensor Combination Attached Or Unattached

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-01-09
• Device Publish Date: 2025-01-01