Gt Metabolic Solutions, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gt Metabolic Solutions, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GT Metabolic MagDI System (MAG-01, MAG-02, DS-01), MagDI System (MAG-02, DS-01), MagDI System (MAG-01, DS-01)
4
Total
3
Cleared
1
Denied
Gt Metabolic Solutions, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Jose, US.
Latest FDA clearance: Jun 2026. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Gt Metabolic Solutions, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Gt Metabolic Solutions, Inc.
4 devices
Cleared
Jun 04, 2026
GT Metabolic MagDI System (MAG-01, MAG-02, DS-01)
General & Plastic Surgery
253d
Cleared
CT
Feb 28, 2025
MagDI System (MAG-02, DS-01)
General & Plastic Surgery
122d
Cleared
Oct 24, 2024
MagDI System (MAG-01, DS-01)
General & Plastic Surgery
99d
Not Cleared
Jul 02, 2024
MagDI System
General & Plastic Surgery
98d