510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K925240Substantially Equivalent

Facebow

Forestadent Bernhard Forster GmbH, D-7530 Pforzheim Germany, GR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925240 is the FDA 510(k) clearance record for FACEBOW, a class II device, cleared for Forestadent Bernhard Forster GmbH on under FDA product code DZB (Headgear, Extraoral, Orthodontic). FDA records list 4 510(k) clearances for Forestadent Bernhard Forster GmbH, from to . As of , FDA records show no recalls naming K925240.

Clearance record

Decision date
Received
(245 days to decision)
Product code
DZB Headgear, Extraoral, Orthodontic
Regulation
21 CFR 872.5500
Device class
Class II
Review panel
Dental
Applicant
Forestadent Bernhard Forster GmbH 7530 Pforzheim, D-7530 Pforzheim Germany, GR
510(k) summary
Statement
Third party review
No

Clearances, product code DZB

Trailing 12 months

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

FDA records show no clearances under product code DZB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DZB, 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