Clinical Laserthermia Systems AB
1 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (1)
Registered facilities (1)
- CLINICAL LASERTHERMIA SYSTEMS AB FEI 3012452798 · SE
Recalls & enforcement
- Class IITerminated2021-04-01single use devices labeled as sterile may not have been adequately sterilized
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “Clinical Laserthermia Systems AB — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-10050452-clinical-laserthermia-systems-ab/
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