510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K233252Substantially Equivalent

Straumann CARES Visual and Nova Dental CAD

Straumann USA, LLC, Basel, CH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K233252 is the FDA 510(k) clearance record for Straumann CARES Visual and Nova Dental CAD, a class II device, cleared for Institut Straumann AG on under FDA product code PNP (Dental Abutment Design Software For Dental Laboratory). FDA's definition for product code PNP reads: "The device is intended to aid in the restoration of chewing function by allowing a dental laboratory or dental clinician to design the patient-specific component of a dental abutment (i.e. abutment collar and abutment post) and CAM or...". FDA records list 176 510(k) clearances for Straumann USA, LLC, from to . As of , FDA records show no recalls naming K233252.

Clearance record

Decision date
Received
(455 days to decision)
Product code
PNP Dental Abutment Design Software For Dental Laboratory
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 PNP

Trailing 12 months

FDA records hold no clearances under product code PNP in the trailing twelve months.

FDA records show no clearances under product code PNP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code PNP, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260