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FDA 510(k)

PORTA OP SOLDER M-1

K-Number: K022452 · 2002-09-11

Decision Date2002-09-11
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PORTA OP SOLDER M-1 is the device name listed in this FDA 510(k) record. The listed applicant is Wieland Dental + Technik GmbH & Co. KG. It received FDA 510(k) clearance on 2002-09-11 under 510(k) number K022452. 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 PORTA OP SOLDER M-1?

PORTA OP SOLDER M-1 is a medical device that received FDA 510(k) clearance on 2002-09-11. The listed applicant is Wieland Dental + Technik GmbH & Co. KG. The 510(k) number is K022452.

When did PORTA OP SOLDER M-1 receive FDA 510(k) clearance?

PORTA OP SOLDER M-1 received FDA 510(k) clearance on 2002-09-11, under 510(k) number K022452.

Who is the listed applicant for PORTA OP SOLDER M-1?

The FDA 510(k) record lists Wieland Dental + Technik GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTA OP SOLDER M-1?

The FDA product code for PORTA OP SOLDER M-1 is EJT.

Related Clinical Trials

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.

Other records listing Wieland Dental + Technik GmbH & Co. KG 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.

View all 42 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.

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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