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FDA 510(k)

ACETAL DENTAL/PREFORMED CLASP

K-Number: K955946 · 1995-12-11

ApplicantPressing DI Monticelli Rag. Stefano
Decision Date1995-12-11
Product CodeEHP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACETAL DENTAL/PREFORMED CLASP is the device name listed in this FDA 510(k) record. The listed applicant is Pressing DI Monticelli Rag. Stefano. It received FDA 510(k) clearance on 1995-12-11 under 510(k) number K955946. The device is classified under product code EHP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETAL DENTAL/PREFORMED CLASP?

ACETAL DENTAL/PREFORMED CLASP is a medical device that received FDA 510(k) clearance on 1995-12-11. The listed applicant is Pressing DI Monticelli Rag. Stefano. The 510(k) number is K955946.

When did ACETAL DENTAL/PREFORMED CLASP receive FDA 510(k) clearance?

ACETAL DENTAL/PREFORMED CLASP received FDA 510(k) clearance on 1995-12-11, under 510(k) number K955946.

Who is the listed applicant for ACETAL DENTAL/PREFORMED CLASP?

The FDA 510(k) record lists Pressing DI Monticelli Rag. Stefano as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACETAL DENTAL/PREFORMED CLASP?

The FDA product code for ACETAL DENTAL/PREFORMED CLASP is EHP.

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 Pressing DI Monticelli Rag. Stefano 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.

K973542MASKY

Related Devices (Code: EHP)

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.

K022032ACETALInovativ, LLCK983558ACETAL DENTAL/PREFORMED CLASPDentamax, Inc.K974622DENTAL DMicro Dental LaboratoriesK954971ACETAL DENTAL/PREFORMED CLASPB & H Technical Services , Ltd.K854765INSTA-TOOTH SPLINT BAR WITH & WITHOUT TEETHC&C Systems, Inc.K800574VACUDENT LUMIX 65Vacudent Sales Corp.

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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