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FDA 510(k)

COMPOSITE RESTORATION MATERIAL

K-Number: K031721 · 2003-09-11

ApplicantMilton Hodosh, M.D.
Decision Date2003-09-11
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

COMPOSITE RESTORATION MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Milton Hodosh, M.D.. It received FDA 510(k) clearance on 2003-09-11 under 510(k) number K031721. 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 COMPOSITE RESTORATION MATERIAL?

COMPOSITE RESTORATION MATERIAL is a medical device that received FDA 510(k) clearance on 2003-09-11. The listed applicant is Milton Hodosh, M.D.. The 510(k) number is K031721.

When did COMPOSITE RESTORATION MATERIAL receive FDA 510(k) clearance?

COMPOSITE RESTORATION MATERIAL received FDA 510(k) clearance on 2003-09-11, under 510(k) number K031721.

Who is the listed applicant for COMPOSITE RESTORATION MATERIAL?

The FDA 510(k) record lists Milton Hodosh, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMPOSITE RESTORATION MATERIAL?

The FDA product code for COMPOSITE RESTORATION MATERIAL is EBF.

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Other records listing Milton Hodosh, M.D. 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.

K032175DESENS-IONOMERK022025MODIFICATION TO POTASSIUM NITRATE-POLYCARBOXYLATE DENTAL CEMENTK925207GLASS IONOMER CEMENTK905582POTASSIUM NITRATE COMPOSITE RESTORATION PIT ANDK895988POTASSIUM NITRATE-ZINC OXIDE EUGENOL TEMP. DENTALK882417POTASSIUM NITRATE POLYCARBOXYLATE DENTAL CEMENT

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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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