510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K172798Substantially Equivalent

Straumann CARES Abutments CoCr

Straumann USA, LLC, Basel, CH / Traditional, Substantially Equivalent

K172798 is the FDA 510(k) clearance record for Straumann CARES Abutments CoCr, a class II device, cleared for Institut Straumann AG on under FDA product code NHA (Abutment, Implant, Dental, Endosseous). FDA's definition for product code NHA reads: "To be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation". FDA records list 176 510(k) clearances for Straumann USA, LLC, from to . As of , FDA records show no recalls naming K172798.

Clearance record

Decision date
Received
(107 days to decision)
Product code
NHA Abutment, Implant, Dental, Endosseous
Regulation
21 CFR 872.3630
Device class
Class II
Review panel
Dental
Applicant
Institut Straumann AG Peter Merian Weg 12, Basel, CH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NHA

Trailing 12 months
30 clearances under product code NHA in the twelve months to October 2026, June 2026 the highest month at 6.
Show the numbers
Monthly 510(k) clearances under FDA product code NHA, trailing twelve months
MonthClearances
November 20253
December 20254
January 20265
February 20261
March 20261
April 20262
May 20263
June 20266
July 20261
August 20261
September 20263
October 20260