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FDA 510(k)

DENTAL HANDPIECE

K-Number: K780038 · 1978-01-20

ApplicantLares Manufacturing Co., Inc.
Decision Date1978-01-20
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Lares Manufacturing Co., Inc.. It received FDA 510(k) clearance on 1978-01-20 under 510(k) number K780038. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL HANDPIECE?

DENTAL HANDPIECE is a medical device that received FDA 510(k) clearance on 1978-01-20. The listed applicant is Lares Manufacturing Co., Inc.. The 510(k) number is K780038.

When did DENTAL HANDPIECE receive FDA 510(k) clearance?

DENTAL HANDPIECE received FDA 510(k) clearance on 1978-01-20, under 510(k) number K780038.

Who is the listed applicant for DENTAL HANDPIECE?

The FDA 510(k) record lists Lares Manufacturing Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTAL HANDPIECE?

The FDA product code for DENTAL HANDPIECE is EFB.

Related Clinical Trials

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.

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Other records listing Lares Manufacturing Co., 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.

K831351PERMALUX VISIBLE CURE COMPOSITE RESTORK801535LARES HANDPIECE OILK801592FIBER OPTIC HOSEK801591FIBER OPTIC ILLUMINATORK801534LARES AIR PRESSURE GAUGE

Related Devices (Code: EFB)

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.

K262144DIAMED Handpiece;DIAMED Airmotor;DIAMED Airmotor HandpieceSETAGAYA SEIKI Co., Ltd.K251388Dental air-motor handpiece (TM-203B2, TM-203M4, TM-205B2, TM-205M4, TM-IS, TM-ES, TM-SG20, TM-X25, TM-BB, TM-IC, TM-RA41)Foshan Topmed Dental Co., Ltd.K251389High speed air turbine handpieceFoshan Topmed Dental Co., Ltd.K242179Synea Fusion Handpieces (Intensiv & Profin)W&H Dentalwerk Bürmoos GmbHK240337Dental Handpiece (Model: J6-126, J6-136, SH11W2, SH11W3, W401LW, W15LW, W142LW, W11L)Guangdong Jinme Medical Technology Co., Ltd.K241074High-speed Air Turbine Handpieces (SCHG01, SCHG03, SCHG18, SCHF19, SCHF22), Dental Low Speed Handpieces including Straight and Geared Angle Handpieces and Air Motors (Straight Handpieces: SCHD05-S, SCHD16-S, SCHD17-S, SCHD24-S, SCHD27-S Geared Angle Handpieces: SCHD05-C, SCHD06-C, SCHD16-C, SCHD17-C, SCHD24-C, SCHD27-C, SCHD29-S, SCHB4, SCHB5, SCHB20, SCHB64 Air Motors: SCHD16-M, SCHD17-M, SCHD24-M, SCHD27-M)Foshan Soco Precision Instrument Co., Ltd.

Official Source

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

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