510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K082532Substantially Equivalent

Straumann Guided Instruments

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

K082532 is the FDA 510(k) clearance record for STRAUMANN GUIDED INSTRUMENTS, a class II device, cleared for Straumann USA on under FDA product code DZI (Drill, Bone, Powered). FDA records list 176 510(k) clearances for Straumann USA, from to . As of , FDA records show no recalls naming K082532.

Clearance record

Decision date
Received
(49 days to decision)
Product code
DZI Drill, Bone, Powered
Regulation
21 CFR 872.4120
Device class
Class II
Review panel
Dental
Applicant
Straumann USA 60 Minuteman Rd., Andover MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DZI

Trailing 12 months
3 clearances under product code DZI in the twelve months to November 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DZI, trailing twelve months
MonthClearances
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20261
August 20260
September 20260
October 20260
November 20260