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FDA 510(k)

LW UCLA Abutment

K-Number: K231235 · 2023-09-15

ApplicantOssvis Co., Ltd.
Decision Date2023-09-15
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LW UCLA Abutment is a medical device manufactured by Ossvis Co., Ltd.. It received FDA 510(k) clearance on 2023-09-15 under approval number K231235. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LW UCLA Abutment?

LW UCLA Abutment is a medical device that received FDA 510(k) clearance on 2023-09-15. It is manufactured by Ossvis Co., Ltd.. The 510(k) number is K231235.

When was LW UCLA Abutment approved by the FDA?

LW UCLA Abutment received FDA 510(k) clearance on 2023-09-15, under approval number K231235.

What company makes LW UCLA Abutment?

LW UCLA Abutment is manufactured by Ossvis Co., Ltd..

What is the FDA product code for LW UCLA Abutment?

The FDA product code for LW UCLA Abutment is NHA.

Other Devices by Ossvis Co., Ltd.

K231079LW Retraction Cap K223924LW Implant System K242703LW Pre-milled Abutment K242379LL Implant System K233808LW Narrow Implant System K233167LW Implant System – Abutment

View all 7 devices →

Related Devices (Code: NHA)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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