Class Class II

FiberLocker Implant ; FiberLocker Instrument ; FiberLocker PowerUnit (K253867)

K253867 2026-01-02 Special
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Description

FiberLocker Implant ; FiberLocker Instrument ; FiberLocker PowerUnit by ZuriMED Technologies AG, an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253867
Clearance Date2026-01-02
Clearance TypeSpecial
Product CodeOWX
Regulation Number878.3300

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