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Guenter Bissinger Medizintechnik GmbH

Günter Bissinger Medizintechnik GmbH · Model 85500015 · UDI-DI 04250418722902

KNS Prescription
10
510(k) clearances
17,612
Adverse events (83 deaths)
125
Recalls
117
Facilities

Description

Electrode 3mm tong type bit, 34 cm f. detachable coagulation forceps 34 cm

Recalls

DateFirmReason
2026-08-19Olympus Corporation of the AmericasPotential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
2026-08-19Olympus Corporation of the AmericasPotential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
2026-08-19Olympus Corporation of the AmericasPotential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
2026-08-19Olympus Corporation of the AmericasPotential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
2026-01-07Olympus Corporation of the AmericasDevices which did not undergo thermoforming could deform and lose performance.
2026-01-07Olympus Corporation of the AmericasDevices which did not undergo thermoforming could deform and lose performance.
2026-01-07Olympus Corporation of the AmericasDevices which did not undergo thermoforming could deform and lose performance.
2026-01-07Olympus Corporation of the AmericasDevices which did not undergo thermoforming could deform and lose performance.
2026-01-07Olympus Corporation of the AmericasDevices which did not undergo thermoforming could deform and lose performance.
2026-01-07Olympus Corporation of the AmericasDevices which did not undergo thermoforming could deform and lose performance.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.