Clinical Laserthermia Systems, AB
Clinical Laserthermia Systems, AB holds FDA 510(k) medical device clearances, first cleared 2015, most recent 2025, with 3 FDA device recalls on record.
Top product codes for Clinical Laserthermia Systems, AB
FDA recalls by Clinical Laserthermia Systems, AB
- Z-1781-2021 — Tranberg MR Stylet, 1.8mm/15G, 230mm, REF: 4013-06, Rx Only, Sterile EO - Product Usage: used with the Tranberg¿ MR Introducer; a device used to aid the insertion of the Laser Applicator into the tissue.
- Z-1782-2021 — Tranberg Laser Applicator Non-cooled, 1.7mm/ 15G, 15 mm, Diffuser, 12 m, REF: 4017-02, Rx Only, Sterile EO - Product Usage: used with the Tranberg¿ MR Introducer; a device used to aid the insertion of the Laser Applicator into the tissue.
- Z-1780-2021 — Tranberg MR Cannula, REF: 4013-05, Rx Only, Sterile EO - Product Usage: used with the Tranberg¿ MR Introducer; a device used to aid the insertion of the Laser Applicator into the tissue.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Clinical Laserthermia Systems, AB
Data sourced from openFDA. This site is unofficial and independent of the FDA.