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FDA 510(k)

BRANEMARK SYSTEM HEALING CAPS

K-Number: K925780 · 1993-04-14

ApplicantNobelpharma USA, Inc.
Decision Date1993-04-14
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BRANEMARK SYSTEM HEALING CAPS is the device name listed in this FDA 510(k) record. The listed applicant is Nobelpharma USA, Inc.. It received FDA 510(k) clearance on 1993-04-14 under 510(k) number K925780. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRANEMARK SYSTEM HEALING CAPS?

BRANEMARK SYSTEM HEALING CAPS is a medical device that received FDA 510(k) clearance on 1993-04-14. The listed applicant is Nobelpharma USA, Inc.. The 510(k) number is K925780.

When did BRANEMARK SYSTEM HEALING CAPS receive FDA 510(k) clearance?

BRANEMARK SYSTEM HEALING CAPS received FDA 510(k) clearance on 1993-04-14, under 510(k) number K925780.

Who is the listed applicant for BRANEMARK SYSTEM HEALING CAPS?

The FDA 510(k) record lists Nobelpharma USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BRANEMARK SYSTEM HEALING CAPS?

The FDA product code for BRANEMARK SYSTEM HEALING CAPS is DZE.

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Other records listing Nobelpharma USA, Inc. 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.

K984162BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM FOR PEDIATRIC USEK962403NOBLEPHARMA WIDE ACCESSORIESK955713NOBELPHARMA BONE ANCHORED HEARING AIDK962130BRANEMARK SYSTEMS MKII SELK-TAPPING FIXTUREK96173617 ANGULATED ABUTMENTK961737CERA ONE ABUTMENT SYSTEM

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Related Devices (Code: DZE)

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

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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