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FDA 510(k)

PONTOR MPF,V-GNATHOS PF,24K CASTING GOLD

K-Number: K915111 · 1992-01-31

ApplicantMetalor Dental USA Corp.
Decision Date1992-01-31
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PONTOR MPF,V-GNATHOS PF,24K CASTING GOLD is the device name listed in this FDA 510(k) record. The listed applicant is Metalor Dental USA Corp.. It received FDA 510(k) clearance on 1992-01-31 under 510(k) number K915111. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PONTOR MPF,V-GNATHOS PF,24K CASTING GOLD?

PONTOR MPF,V-GNATHOS PF,24K CASTING GOLD is a medical device that received FDA 510(k) clearance on 1992-01-31. The listed applicant is Metalor Dental USA Corp.. The 510(k) number is K915111.

When did PONTOR MPF,V-GNATHOS PF,24K CASTING GOLD receive FDA 510(k) clearance?

PONTOR MPF,V-GNATHOS PF,24K CASTING GOLD received FDA 510(k) clearance on 1992-01-31, under 510(k) number K915111.

Who is the listed applicant for PONTOR MPF,V-GNATHOS PF,24K CASTING GOLD?

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

What is the FDA product code for PONTOR MPF,V-GNATHOS PF,24K CASTING GOLD?

The FDA product code for PONTOR MPF,V-GNATHOS PF,24K CASTING GOLD is EJT.

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Other records listing Metalor Dental USA 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.

K003387AUROFILM NPK993475AUROFLUID M, ALLOY NO. 5315K993505V-DELTA SPECIAL, ALLOY NO. 5154K993506PAGALINOR 4 , ALLOY NO. 5440K993507V-SUPRAGOLD, ALLOY NO. 5024K993508V-SUPRA PLUS, ALLOY NO. 5025

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Related Devices (Code: EJT)

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.

K052463PROMETAL HN86Prometal TechnologiesK041378BIO 60Kodent, Inc.K040672PORTA REFLEXWieland Dental + Technik GmbH & Co. KGK040524PORTA SOLDER 1090 WWieland Dental + Technik GmbH & Co. KGK040043NDX-40 ALLOYHeraeus Kulzer, Inc.K034049HERADOR EC, PF, C, H, NH, G, GG AND MP; HERALOY U AND G; HERABOND N; ALBABOND C, B AND A; BIO HERANORMHeraeus Kulzer,GmbH

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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