510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K890721Substantially Equivalent

Shape-Actio Metal Toxicology Control

Actio, Inc., Oakland CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890721 is the FDA 510(k) clearance record for SHAPE-ACTIO METAL TOXICOLOGY CONTROL, a class I device, cleared for Actio, Inc. on under FDA product code DIE (Heavy Metals Control Materials). FDA records list 4 510(k) clearances for Actio, Inc., from to . As of , FDA records show no recalls naming K890721.

Clearance record

Decision date
Received
(56 days to decision)
Product code
DIE Heavy Metals Control Materials
Regulation
21 CFR 862.3280
Device class
Class I
Review panel
Clinical Toxicology
Applicant
Actio, Inc. 1127-57th Ave., Oakland CA
Third party review
No

Clearances, product code DIE

Trailing 12 months

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

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