Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ALPHALOK™ Plating System

K-Number: K212348 · 2022-05-02

ApplicantVilex, LLC
Decision Date2022-05-02
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALPHALOK™ Plating System is the device name listed in this FDA 510(k) record. The listed applicant is Vilex, LLC. It received FDA 510(k) clearance on 2022-05-02 under 510(k) number K212348. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALPHALOK™ Plating System?

ALPHALOK™ Plating System is a medical device that received FDA 510(k) clearance on 2022-05-02. The listed applicant is Vilex, LLC. The 510(k) number is K212348.

When did ALPHALOK™ Plating System receive FDA 510(k) clearance?

ALPHALOK™ Plating System received FDA 510(k) clearance on 2022-05-02, under 510(k) number K212348.

Who is the listed applicant for ALPHALOK™ Plating System?

The FDA 510(k) record lists Vilex, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALPHALOK™ Plating System?

The FDA product code for ALPHALOK™ Plating System is HRS.

Other records listing Vilex, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260900DYNEX® External Fixation SystemsK250304TITANEX Screw SystemsK240475Hintermann Series H2 Total Ankle SystemK243408TACTIX Vector Syndesmosis SystemK233816REDEMPTION Charcot Plating SystemK240035TACTIX Vector Syndesmosis System

View all 17 devices →

Related Devices (Code: HRS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260277MIKRON TRAUMA BONE PLATE& SCREW SYSTEMMikron Makina San. ve Tic. Ltd. Sti.K261511Xpert AnkleNewclip TechnicsK261406Versalock Proximal Tibial Plating SystemGM Dos Reis Industria e Comercio Ltda.K262032TriMed Non-Spanning Wrist Fusion Plates (NSFL-STD);TriMed Non-Spanning Wrist Fusion Plates (NSFR-STD);TriMed Non-Spanning Wrist Fusion Plates (NSFL-SHB );TriMed Non-Spanning Wrist Fusion Plates (NSFR-SHB )TriMed, Inc.K261191Alians Elbow SNewclip TechnicsK261054RibPlate SystemStryker Leibinger GmbH & Co KG

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.

↑