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FDA 510(k)

LANG DENTAL RESINCAP PATTERN AND COPING ACRYLIC RESIN

K-Number: K081705 · 2008-09-17

Decision Date2008-09-17
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LANG DENTAL RESINCAP PATTERN AND COPING ACRYLIC RESIN is the device name listed in this FDA 510(k) record. The listed applicant is Lang Dental Mfg. Co., Inc.. It received FDA 510(k) clearance on 2008-09-17 under 510(k) number K081705. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANG DENTAL RESINCAP PATTERN AND COPING ACRYLIC RESIN?

LANG DENTAL RESINCAP PATTERN AND COPING ACRYLIC RESIN is a medical device that received FDA 510(k) clearance on 2008-09-17. The listed applicant is Lang Dental Mfg. Co., Inc.. The 510(k) number is K081705.

When did LANG DENTAL RESINCAP PATTERN AND COPING ACRYLIC RESIN receive FDA 510(k) clearance?

LANG DENTAL RESINCAP PATTERN AND COPING ACRYLIC RESIN received FDA 510(k) clearance on 2008-09-17, under 510(k) number K081705.

Who is the listed applicant for LANG DENTAL RESINCAP PATTERN AND COPING ACRYLIC RESIN?

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

What is the FDA product code for LANG DENTAL RESINCAP PATTERN AND COPING ACRYLIC RESIN?

The FDA product code for LANG DENTAL RESINCAP PATTERN AND COPING ACRYLIC RESIN is EBG.

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.

Other records listing Lang Dental Mfg. 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.

View all 9 devices →

Related Devices (Code: EBG)

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.

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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