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FDA 510(k)

VS11 SF

K-Number: K951271 · 1995-06-22

ApplicantMetalor Dental USA Corp.
Decision Date1995-06-22
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VS11 SF 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 1995-06-22 under 510(k) number K951271. 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 VS11 SF?

VS11 SF is a medical device that received FDA 510(k) clearance on 1995-06-22. The listed applicant is Metalor Dental USA Corp.. The 510(k) number is K951271.

When did VS11 SF receive FDA 510(k) clearance?

VS11 SF received FDA 510(k) clearance on 1995-06-22, under 510(k) number K951271.

Who is the listed applicant for VS11 SF?

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 VS11 SF?

The FDA product code for VS11 SF is EJT.

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. 5440K993508V-SUPRA PLUS, ALLOY NO. 5025K993507V-SUPRAGOLD, ALLOY NO. 5024

View all 67 devices →

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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