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FDA 510(k)

PERIOFLEX TIP

K-Number: K923711 · 1994-05-16

ApplicantNovadent, Ltd.
Decision Date1994-05-16
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERIOFLEX TIP is the device name listed in this FDA 510(k) record. The listed applicant is Novadent, Ltd.. It received FDA 510(k) clearance on 1994-05-16 under 510(k) number K923711. The device is classified under product code EFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIOFLEX TIP?

PERIOFLEX TIP is a medical device that received FDA 510(k) clearance on 1994-05-16. The listed applicant is Novadent, Ltd.. The 510(k) number is K923711.

When did PERIOFLEX TIP receive FDA 510(k) clearance?

PERIOFLEX TIP received FDA 510(k) clearance on 1994-05-16, under 510(k) number K923711.

Who is the listed applicant for PERIOFLEX TIP?

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

What is the FDA product code for PERIOFLEX TIP?

The FDA product code for PERIOFLEX TIP is EFS.

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Related Devices (Code: EFS)

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.

K023232SPLATRFREE SWANGLE 360 DISPOSABLE PROPHYLAXIS ANGLESmartpracticeK001493DENTAL AIR FORCE HOME DENTAL CLEANING SYSTEM, MODEL NO. 0020001Air Force, Inc.K983374AGATHA-A-H2010Midian Intl.K964810DERMADAMUltradent Products, Inc.K952234BARRIER ALL FILMCottrell, Ltd.K943182ORAL-B PERIOFLEX SUBGINGIVAL IRRIGATOROral-B Laboratories

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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