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FDA 510(k)

AMERICAN DENTAL PRODUCTS (ADP), COMPOSITE RESTORATIVE MATERIAL

K-Number: K951427 · 1995-05-15

ApplicantAmerican Dental Products, Inc.
Decision Date1995-05-15
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AMERICAN DENTAL PRODUCTS (ADP), COMPOSITE RESTORATIVE MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is American Dental Products, Inc.. It received FDA 510(k) clearance on 1995-05-15 under 510(k) number K951427. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMERICAN DENTAL PRODUCTS (ADP), COMPOSITE RESTORATIVE MATERIAL?

AMERICAN DENTAL PRODUCTS (ADP), COMPOSITE RESTORATIVE MATERIAL is a medical device that received FDA 510(k) clearance on 1995-05-15. The listed applicant is American Dental Products, Inc.. The 510(k) number is K951427.

When did AMERICAN DENTAL PRODUCTS (ADP), COMPOSITE RESTORATIVE MATERIAL receive FDA 510(k) clearance?

AMERICAN DENTAL PRODUCTS (ADP), COMPOSITE RESTORATIVE MATERIAL received FDA 510(k) clearance on 1995-05-15, under 510(k) number K951427.

Who is the listed applicant for AMERICAN DENTAL PRODUCTS (ADP), COMPOSITE RESTORATIVE MATERIAL?

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

What is the FDA product code for AMERICAN DENTAL PRODUCTS (ADP), COMPOSITE RESTORATIVE MATERIAL?

The FDA product code for AMERICAN DENTAL PRODUCTS (ADP), COMPOSITE RESTORATIVE MATERIAL is EBF.

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Other records listing American Dental Products, 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.

K093014AMERICAN DENTAL PRODUCTS SE BONDEASYK994368AMERICAN DENTAL PRODUCTS CARIES-DETECTOR PLUSK991099AMERICAN DENTAL PRODUCTS ETCH-DETECTK973185AMERICAN DENTAL PRODUCTS HB-35 DESENSITIZER WITH FLUORIDEK964133AMERICAN DENTAL PRODUCTS HG 35 DESENSITIZER WITH FLUORIDEK954637AMERICAN DENTAL PRODUCTS TISSUE CONDITIONER & TEMPORARY RELINER

View all 23 devices →

Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, 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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