510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K810220Substantially Equivalent

Powered Patient System

Tri W-G, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K810220 is the FDA 510(k) clearance record for POWERED PATIENT SYSTEM, a class II device, cleared for Tri W-G, Inc. on under FDA product code IKZ (Bed, Patient Rotation, Powered). FDA records list 35 510(k) clearances for Tri W-G, Inc., from to . As of , FDA records show no recalls naming K810220.

Clearance record

Decision date
Received
(8 days to decision)
Product code
IKZ Bed, Patient Rotation, Powered
Regulation
21 CFR 890.5225
Device class
Class II
Review panel
Physical Medicine
Applicant
Tri W-G, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code IKZ

Trailing 12 months

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

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