Modular Medical Submits Pivot Tubeless Insulin Patch Pump for FDA 510(k) Review

Reuters

2025/11/14

Modular Medical Submits Pivot Tubeless Insulin Patch Pump for FDA 510(k) Review

Modular Medical Inc. has announced the submission of its next generation Pivot™ tubeless insulin patch pump for FDA 510(k) clearance. The company expects to receive initial questions from the FDA in the fourth quarter of 2025 and is preparing for a commercial launch in the first quarter of 2026, pending regulatory approval. The Pivot system is not yet cleared for sale by the FDA. No grant or funding announcement involving multiple organizations was included.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Modular Medical Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. ID: 1102238) on November 14, 2025, and is solely responsible for the information contained therein.

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