CMT Health PTE., Ltd. is one of 29 FDA 510(k) medical device manufacturers from Singapore in the dataset, ranked by real submission volume.
CMT Health PTE., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Profoject Enteral/Oral Feeding Syringe, Profoject™ Insulin Syringes, Profoject™ Low Dead Space Syringe /Profoject™ Tuberculin Syringe
10
Total
10
Cleared
0
Denied
CMT Health PTE., Ltd. has 10 FDA 510(k) cleared general hospital devices. Based in Singapore, SG.
Latest FDA clearance: Jul 2026. Active since 2025.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - CMT Health PTE., Ltd.
10 devices
Cleared
Jul 29, 2026
Profoject™ Dual-Safety Pen Needles
General Hospital
57d
Cleared
Jul 15, 2026
Profoject™ Pen Needles (Model A
General Hospital
131d
Cleared
Jun 12, 2026
Profoject™ Safety Needle
General Hospital
115d
Cleared
Jun 10, 2026
Profoject™ Safety Pen Needles
General Hospital
86d
Cleared
Apr 08, 2026
Profoject Enteral/Oral Feeding Syringe
Gastroenterology & Urology
191d
Cleared
Feb 23, 2026
Profoject™ Insulin Syringes
General Hospital
154d
Cleared
Feb 19, 2026
Profoject™ Low Dead Space Syringe /Profoject™ Tuberculin Syringe
General Hospital
168d
Cleared
Oct 16, 2025
Profoject™ Disposable Needle
General Hospital
57d
Cleared
Jul 25, 2025
Profoject™ Disposable Syringe, Profoject™ Disposable Syringe with Needle
General Hospital
25d
Cleared
Jul 18, 2025
Profoject™ Enteral Feeding Syringe
Gastroenterology & Urology
56d