510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K780890Substantially Equivalent

Capp Terminal Device

Hosmer Dorrance Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K780890 is the FDA 510(k) clearance record for CAPP TERMINAL DEVICE, a class I device, cleared for Hosmer Dorrance Corp. on under FDA product code IQX (Hook, External Limb Component, Mechanical). FDA records list 9 510(k) clearances for Hosmer Dorrance Corp., from to . As of , FDA records show no recalls naming K780890.

Clearance record

Decision date
Received
(13 days to decision)
Product code
IQX Hook, External Limb Component, Mechanical
Regulation
21 CFR 890.3420
Device class
Class I
Review panel
Physical Medicine
Applicant
Hosmer Dorrance Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code IQX

Trailing 12 months

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

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