Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS

K-Number: K913089 · 1992-04-21

ApplicantWilde-USA, Inc.
Decision Date1992-04-21
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS is the device name listed in this FDA 510(k) record. The listed applicant is Wilde-USA, Inc.. It received FDA 510(k) clearance on 1992-04-21 under 510(k) number K913089. 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 WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS?

WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS is a medical device that received FDA 510(k) clearance on 1992-04-21. The listed applicant is Wilde-USA, Inc.. The 510(k) number is K913089.

When did WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS receive FDA 510(k) clearance?

WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS received FDA 510(k) clearance on 1992-04-21, under 510(k) number K913089.

Who is the listed applicant for WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS?

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

What is the FDA product code for WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS?

The FDA product code for WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS is EBF.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Wilde-USA, 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.

K913582COMPATIT RK915653KERAMAILK913581WILDE ADHESIVE BONDING SYSTEMK923472COMPACOLORK920649COMPASEPK915250WIL-PDS & WIL-PDI CASTING ALLOYS

View all 16 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.

↑