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FDA 510(k)

FLEX SPAN TEMPORARY CROWN & BRIDGE MATERIAL

K-Number: K021457 · 2002-08-01

ApplicantPentron Corp.
Decision Date2002-08-01
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLEX SPAN TEMPORARY CROWN & BRIDGE MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Pentron Corp.. It received FDA 510(k) clearance on 2002-08-01 under 510(k) number K021457. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEX SPAN TEMPORARY CROWN & BRIDGE MATERIAL?

FLEX SPAN TEMPORARY CROWN & BRIDGE MATERIAL is a medical device that received FDA 510(k) clearance on 2002-08-01. The listed applicant is Pentron Corp.. The 510(k) number is K021457.

When did FLEX SPAN TEMPORARY CROWN & BRIDGE MATERIAL receive FDA 510(k) clearance?

FLEX SPAN TEMPORARY CROWN & BRIDGE MATERIAL received FDA 510(k) clearance on 2002-08-01, under 510(k) number K021457.

Who is the listed applicant for FLEX SPAN TEMPORARY CROWN & BRIDGE MATERIAL?

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

What is the FDA product code for FLEX SPAN TEMPORARY CROWN & BRIDGE MATERIAL?

The FDA product code for FLEX SPAN TEMPORARY CROWN & BRIDGE MATERIAL is EBG.

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.

Other records listing Pentron 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.

View all 15 devices →

Related Devices (Code: EBG)

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.

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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