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FDA 510(k)

JEDENTAL VLC DENTAL CURING LIGHT

K-Number: K935718 · 1994-01-26

ApplicantJedental Co., Inc.
Decision Date1994-01-26
Product CodeEAY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JEDENTAL VLC DENTAL CURING LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Jedental Co., Inc.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K935718. The device is classified under product code EAY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JEDENTAL VLC DENTAL CURING LIGHT?

JEDENTAL VLC DENTAL CURING LIGHT is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Jedental Co., Inc.. The 510(k) number is K935718.

When did JEDENTAL VLC DENTAL CURING LIGHT receive FDA 510(k) clearance?

JEDENTAL VLC DENTAL CURING LIGHT received FDA 510(k) clearance on 1994-01-26, under 510(k) number K935718.

Who is the listed applicant for JEDENTAL VLC DENTAL CURING LIGHT?

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

What is the FDA product code for JEDENTAL VLC DENTAL CURING LIGHT?

The FDA product code for JEDENTAL VLC DENTAL CURING LIGHT is EAY.

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Other records listing Jedental 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.

K933612JEDENTAL;PCA CEMENT (POLYCARBOXYLATE CEMENT)K934073JEDENTAL GLASS IONOMER CEMENT AND LINERK935727P&FS PIT AND FISSURE SEALANTK933656JEDENTAL PSROFILL SELF-CURE COMPOSITEK933554JEDENTAL ZINC CEMENT IMPROVEDK933543ZOE CEMENT (ZINC OXIDE & EUGENOL CEMENT)

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Related Devices (Code: EAY)

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.

K953192MODEL A15-103Beaverstate Dental, Inc.K953191MODEL A15-101Beaverstate Dental, Inc.K871816STRYKERSCOPE TM/ORTHOSCOPE TM/STRYKER MINISCOPE TMStryker Corp.K831976POWER OPTICRitter Co.K831824DENTAL ELECTRONIC/S.B.R TRADING BU HANDSilverman'SK820907DENTISCOPEChayes Virginia, Inc.

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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