FDA 510(k)

VILA

K-Number: K951381 · 1995-04-27

Decision Date1995-04-27

Product CodeDYH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

VILA is the device name listed in this FDA 510(k) record. The listed applicant is Health-Dent Intl., Inc.. It received FDA 510(k) clearance on 1995-04-27 under 510(k) number K951381. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VILA?

VILA is a medical device that received FDA 510(k) clearance on 1995-04-27. The listed applicant is Health-Dent Intl., Inc.. The 510(k) number is K951381.

When did VILA receive FDA 510(k) clearance?

VILA received FDA 510(k) clearance on 1995-04-27, under 510(k) number K951381.

Who is the listed applicant for VILA?

The FDA 510(k) record lists Health-Dent Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VILA?

The FDA product code for VILA is DYH.

Other records listing Health-Dent Intl., Inc. 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.

K972198DENT-TEMP ACRYLIC K953405HEMA-BENZ K951220HEMA-GLU K951380VILA PC K951235GIROC K951236PRO-LOCK

View all 8 devices →

Related Devices (Code: DYH)

K261129OrthoFitSpident Co., Ltd.K261840BracePaste Prime PlusAmerican Orthodontics K250015Ormco™ EtchFree Bonding System, Ormco™ EtchFree Bonding Primer, Ormco™ EtchFree AdhesiveOrmco Corporation K242537BracePaste Fluoride SealantAmerican Orthodontics Corp.K2340433M™ Transbond™ Orthodontic Adhesive3M Unitek Orthodontic Products K231817AlignerFlow LCVoco GmbH

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.