LANG DENTAL RESINCAP PATTERN AND COPING ACRYLIC RESIN
K-Number: K081705 · 2008-09-17
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Device Summary
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.
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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