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Ossvis Co., Ltd.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7
Categories2
Latest FDA decision2024-12-05
TypeNumberDevice NameCodeDateActions
510(k) K242703 LW Pre-milled AbutmentNHA2024-12-05 View
510(k) K242379 LL Implant SystemDZE2024-11-07 View
510(k) K233808 LW Narrow Implant SystemDZE2024-07-31 View
510(k) K233167 LW Implant System – AbutmentNHA2024-03-25 View
510(k) K231235 LW UCLA AbutmentNHA2023-09-15 View
510(k) K231079 LW Retraction CapNHA2023-09-14 View
510(k) K223924 LW Implant SystemDZE2023-08-08 View
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