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FDA 510(k)

THERMAPOST ENDODONTIC ROOT CANAL POST

K-Number: K922931 · 1994-05-26

ApplicantTulsa Dental Products, Ltd.
Decision Date1994-05-26
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THERMAPOST ENDODONTIC ROOT CANAL POST is the device name listed in this FDA 510(k) record. The listed applicant is Tulsa Dental Products, Ltd.. It received FDA 510(k) clearance on 1994-05-26 under 510(k) number K922931. The device is classified under product code ELR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMAPOST ENDODONTIC ROOT CANAL POST?

THERMAPOST ENDODONTIC ROOT CANAL POST is a medical device that received FDA 510(k) clearance on 1994-05-26. The listed applicant is Tulsa Dental Products, Ltd.. The 510(k) number is K922931.

When did THERMAPOST ENDODONTIC ROOT CANAL POST receive FDA 510(k) clearance?

THERMAPOST ENDODONTIC ROOT CANAL POST received FDA 510(k) clearance on 1994-05-26, under 510(k) number K922931.

Who is the listed applicant for THERMAPOST ENDODONTIC ROOT CANAL POST?

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

What is the FDA product code for THERMAPOST ENDODONTIC ROOT CANAL POST?

The FDA product code for THERMAPOST ENDODONTIC ROOT CANAL POST is ELR.

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Other records listing Tulsa Dental Products, Ltd. 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.

K970134THERMAPREP PLUS OVENK964174MINERAL TRIOXIDE AGGREGATE (MTA)K954790PROFILE NICKEL TITANIUM ROTARY INSTRUMENTSK933582PROFILE SERIES 29 FILESK910224THERMAPREPK900986THERMAFIL ENDODONTIC OBTURATOR

View all 8 devices →

Related Devices (Code: ELR)

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.

K060075FIBER-METAL POSTForemost Dental, LLCK042848FRC POSTEC PLUSIvoclar Vivadent, Inc.K030820EVERSTICK POSTStick Tech , Ltd.K020431FIBIOCOREEst. AnthogyrK012496CARBON POSTJ. Morita USA, Inc.K013802FRC POSTECIvoclar Vivadent, 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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