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Elucid raises $55M Series D with FFR-CT 510(k) under FDA review Enovis to buy eCential Robotics for 155 million euros FDA authorizes Vitestro's Aletta, the first autonomous blood-drawing robot, five months after a $70M Series B Renata Medical raises $25M Series D to scale the Minima pediatric stent FDA opens a docket on how to regulate generative AI devices FDA clears Jupiter Endovascular's Vertex thrombectomy system for pulmonary embolism in 89 days FDA clears Wandercraft's Eve, the first self-balancing exoskeleton for home use Meduloc raises $4M Series B to start alpha launch of its nitinol fracture implant FDA sets FY2027 device user fees: $28,653 for a 510(k), $13,785 to register Elucid raises $55M Series D with FFR-CT 510(k) under FDA review Enovis to buy eCential Robotics for 155 million euros FDA authorizes Vitestro's Aletta, the first autonomous blood-drawing robot, five months after a $70M Series B Renata Medical raises $25M Series D to scale the Minima pediatric stent FDA opens a docket on how to regulate generative AI devices FDA clears Jupiter Endovascular's Vertex thrombectomy system for pulmonary embolism in 89 days FDA clears Wandercraft's Eve, the first self-balancing exoskeleton for home use Meduloc raises $4M Series B to start alpha launch of its nitinol fracture implant FDA sets FY2027 device user fees: $28,653 for a 510(k), $13,785 to register

The Tracker / September 2025 / K251100

510(k) cleared

IPGTFL-02

Ipg Medical Corporation · Sep 19, 2025 · K251100

FDA cleared the IPGTFL-02 from Ipg Medical Corporation on Sep 19, 2025 under K251100, a traditional 510(k). The device falls under product code GEX, Powered Laser Surgical Instrument, regulated at 21 CFR 878.4810 as a Class 2 device. The review panel was General, Plastic Surgery.

FDA logged the submission as received on Apr 10, 2025. The decision came 162 days later, longer than the 90 FDA-day review goal, which usually means at least one additional information request.

This is the only decision on file for Ipg Medical Corporation in the last 12 months of the tracker.

Questions & Answers

What did FDA clear under K251100?

K251100 is the FDA 510(k) for IPGTFL-02, submitted by Ipg Medical Corporation. FDA's decision date was Sep 19, 2025, under product code GEX (Powered Laser Surgical Instrument).

Who makes the IPGTFL-02?

Ipg Medical Corporation, based in Marlborough, MA, is the applicant of record for K251100.

How long did the K251100 review take?

FDA received the submission on Apr 10, 2025 and issued its decision on Sep 19, 2025, 162 days later.

← All decisions in September 2025