Philippines

SOMNOMED INC. has registered two products under code PLC with the FDA.

Terumo (Philippines) Corporation has registered a medical device with product code FMF.

The FDA lifted the public health warning on an unnotified medical device, the Long Bone Plaster Bandage.

The FDA warns against using the unnotified medical device 'PRIME BROWN™ ELASTIC BANDAGE REF.BB10'.

FDA warns against counterfeit Ulthera® System, highlighting public health risks in medical devices.

FDA warns against unregistered medical devices, impacting safety in North America and beyond.

FDA PH Advisory: Lifting of the FDA Advisory No. 2021-1678 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product Long Bone Plaster of Paris Bandage (6” x 5y )” - fda.gov.ph

FDA PH Advisory: FDA Advisory No.2023-0364 || Public Health Warning Against the Purchase and Use of Counterfeit Medical Device “Ulthera® System” - Food and Drug Administration - fda.gov.ph

LeMaitre will participate in the Needham Virtual MedTech & Diagnostics Conference, highlighting industry engagement.

FDA PH Advisory: FDA Advisory No.2026-0675 || Public Health Warning Against the Purchase and Use of the Medical Device Product “HEXACARE DISPOSABLE INFUSION SET NON-PYROGENIC, NON-TOXIC, ADULT” with Expired Certificate of Product Registration (CPR) - fda.gov.ph

FDA PH Advisory: FDA Advisory No.2024-1105 || Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “BERKLEY JENSEN® BANDAGES” - Food and Drug Administration - fda.gov.ph

FDA PH Advisory: Lifting of the FDA Advisory No. 2023-1596 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “R&R REXI CARE ICE/HOT BAG”” - fda.gov.ph