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FDA 510(k)

STRAUMANN COMPUTER AIDED RESTORATION SERVICE

K-Number: K052272 · 2006-01-03

ApplicantStraumann USA
Decision Date2006-01-03
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STRAUMANN COMPUTER AIDED RESTORATION SERVICE is the device name listed in this FDA 510(k) record. The listed applicant is Straumann USA. It received FDA 510(k) clearance on 2006-01-03 under 510(k) number K052272. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRAUMANN COMPUTER AIDED RESTORATION SERVICE?

STRAUMANN COMPUTER AIDED RESTORATION SERVICE is a medical device that received FDA 510(k) clearance on 2006-01-03. The listed applicant is Straumann USA. The 510(k) number is K052272.

When did STRAUMANN COMPUTER AIDED RESTORATION SERVICE receive FDA 510(k) clearance?

STRAUMANN COMPUTER AIDED RESTORATION SERVICE received FDA 510(k) clearance on 2006-01-03, under 510(k) number K052272.

Who is the listed applicant for STRAUMANN COMPUTER AIDED RESTORATION SERVICE?

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

What is the FDA product code for STRAUMANN COMPUTER AIDED RESTORATION SERVICE?

The FDA product code for STRAUMANN COMPUTER AIDED RESTORATION SERVICE is NHA.

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Other records listing Straumann USA as applicant

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K151328PURE Ceramic ImplantsK130724CODIAGNOSTIX IMPLANT PLANNING SOFTWAREK130808STRAUMANN HEALING ABUTMENTS, HEALING CAPS, CLOSURE SCREWSK122855TL 04.1MM RN,S, SLACTIVE TIZR 6, 8, 10, 12, 14, 16MM DENTAL IMPLANTSK121131BL, 04.1 MM RC, SLACTIVE 8MM, TIZR AND 10MM, 12, 14MMK113606NNC GOLD ABUTMENT FOR BRIDGES

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Related Devices (Code: NHA)

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.

K262207Cemented Plus AbutmentUnidental Co., Ltd.K260940BellaTek BarsZimVie US Corp, LLCK253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic ScrewNobel Biocare ABK261147Neodent Implant System - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLCK260061BioHorizons CEREC Compatible Ti-BasesBioHorizons Implant Systems, 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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