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FDA 510(k)

DENTORIUM CONVERTIBLE ACRYLIC

K-Number: K011820 · 2001-09-05

ApplicantNats Corp.
Decision Date2001-09-05
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTORIUM CONVERTIBLE ACRYLIC is the device name listed in this FDA 510(k) record. The listed applicant is Nats Corp.. It received FDA 510(k) clearance on 2001-09-05 under 510(k) number K011820. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTORIUM CONVERTIBLE ACRYLIC?

DENTORIUM CONVERTIBLE ACRYLIC is a medical device that received FDA 510(k) clearance on 2001-09-05. The listed applicant is Nats Corp.. The 510(k) number is K011820.

When did DENTORIUM CONVERTIBLE ACRYLIC receive FDA 510(k) clearance?

DENTORIUM CONVERTIBLE ACRYLIC received FDA 510(k) clearance on 2001-09-05, under 510(k) number K011820.

Who is the listed applicant for DENTORIUM CONVERTIBLE ACRYLIC?

The FDA 510(k) record lists Nats Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTORIUM CONVERTIBLE ACRYLIC?

The FDA product code for DENTORIUM CONVERTIBLE ACRYLIC is EBI.

Related Clinical Trials

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Other records listing Nats Corp. 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.

K040143MONORAILK033142POWERED WHEELCHAIRK020060ASTOFLOK991184HYDROTONE-THERMAL CAPSULE SYSTEM

Related Devices (Code: EBI)

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.

K261802Glidewell™ Denture Base ResinPrismatik Dentalcraft, Inc.K261626UltraPrint Flexible Denture UVGuangzhou Heygears IMC., Inc.K262681NanoCeram Resin3BFAB TEKNOLOJI A.S.K262300Denture Base Resin V2Formlabs Ohio, Inc.K261474DENTCA Tru FlexibleDentca, Inc.K260569DB 4000 High Impact Denture BaseCarbon, 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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