Candela Corporation
2 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (2)
- Inspections (1)
Devices registered here (1)
- Powered Laser Surgical InstrumentProduct code GEX (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.4810
Recalls & enforcement
- Class IITerminated2019-09-10The canister neck bushing may become loose and separate from the body of the canister during use. The issue occurs only when the canisters are used in Candela legacy devices that utilize screw-in or threaded interface type DCD modules
- Class IITerminated2013-11-06Unintended single pulse maybe emitted to handpiece prior to pressing of trigger or footswitch and cause injury.
FDA inspections (1)
- VAI2023-01-24Voluntary Action Indicated · Radiation Control and Health Safety Act · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Candela Corporation (FEI 3016496662) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3016496662-candela-corporation/
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