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FDA 510(k)

BIOBOND C&B POST SOLDER

K-Number: K770009 · 1977-01-10

ApplicantDentsply Intl.
Decision Date1977-01-10
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BIOBOND C&B POST SOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1977-01-10 under 510(k) number K770009. 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 BIOBOND C&B POST SOLDER?

BIOBOND C&B POST SOLDER is a medical device that received FDA 510(k) clearance on 1977-01-10. The listed applicant is Dentsply Intl.. The 510(k) number is K770009.

When did BIOBOND C&B POST SOLDER receive FDA 510(k) clearance?

BIOBOND C&B POST SOLDER received FDA 510(k) clearance on 1977-01-10, under 510(k) number K770009.

Who is the listed applicant for BIOBOND C&B POST SOLDER?

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

What is the FDA product code for BIOBOND C&B POST SOLDER?

The FDA product code for BIOBOND C&B POST SOLDER is EJT.

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Other records listing Dentsply Intl. as applicant

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K123615IRIS - HIGH STRENGTH GLASS CERAMICK072730FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTSK070538XP BOND DUAL CURE UNIVERSAL TOTAL ETCH ADHESIVEK070019CARRARA VOLUMIAK061427PRE-IMPRESSION CONDITIONING SOLUTIONK052334CAVITRON RF ULTRASONIC SCALER SYSTEM WITH STERIMATE HANDPIECE, MODEL G-131

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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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