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FDA 510(k)

Master-Pin X (MP Pin with thread) (36BMP000030 / MP30)

K-Number: K250123 · 2025-09-29

Decision Date2025-09-29
Product CodeDZL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Master-Pin X (MP Pin with thread) (36BMP000030 / MP30) is the device name listed in this FDA 510(k) record. The listed applicant is Hager& Meisinger GmbH. It received FDA 510(k) clearance on 2025-09-29 under 510(k) number K250123. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Master-Pin X (MP Pin with thread) (36BMP000030 / MP30)?

Master-Pin X (MP Pin with thread) (36BMP000030 / MP30) is a medical device that received FDA 510(k) clearance on 2025-09-29. The listed applicant is Hager& Meisinger GmbH. The 510(k) number is K250123.

When did Master-Pin X (MP Pin with thread) (36BMP000030 / MP30) receive FDA 510(k) clearance?

Master-Pin X (MP Pin with thread) (36BMP000030 / MP30) received FDA 510(k) clearance on 2025-09-29, under 510(k) number K250123.

Who is the listed applicant for Master-Pin X (MP Pin with thread) (36BMP000030 / MP30)?

The FDA 510(k) record lists Hager& Meisinger GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Master-Pin X (MP Pin with thread) (36BMP000030 / MP30)?

The FDA product code for Master-Pin X (MP Pin with thread) (36BMP000030 / MP30) is DZL.

Other records listing Hager& Meisinger GmbH 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 8 devices →

Related Devices (Code: DZL)

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.