510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K842680Substantially Equivalent

Ace Universal Tong

Buckman Co., Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K842680 is the FDA 510(k) clearance record for ACE UNIVERSAL TONG, a class II device, cleared for Buckman Co., Inc. on under FDA product code HAX (Tong, Skull For Traction). FDA records list 111 510(k) clearances for Buckman Co., Inc., from to . As of , FDA records show no recalls naming K842680.

Clearance record

Decision date
Received
(56 days to decision)
Product code
HAX Tong, Skull For Traction
Regulation
21 CFR 882.5960
Device class
Class II
Review panel
Neurology
Applicant
Buckman Co., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HAX

Trailing 12 months

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

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