510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K860553Substantially Equivalent

Storz, Alpha II Biometric Ruler

Storz Instrument Co., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860553 is the FDA 510(k) clearance record for STORZ, ALPHA II BIOMETRIC RULER, a class II device, cleared for Storz Instrument Co. on under FDA product code ITX (Transducer, Ultrasonic, Diagnostic). FDA records list 101 510(k) clearances for Storz Instrument Co., from to . As of , FDA records show no recalls naming K860553.

Clearance record

Decision date
Received
(122 days to decision)
Product code
ITX Transducer, Ultrasonic, Diagnostic
Regulation
21 CFR 892.1570
Device class
Class II
Review panel
Radiology
Applicant
Storz Instrument Co. 3365 Tree Ct. Industrial Blvd., St. Louis MO
Third party review
No

Clearances, product code ITX

Trailing 12 months
6 clearances under product code ITX in the twelve months to October 2026, July 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code ITX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20263
August 20262
September 20261
October 20260