510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K812053Substantially Equivalent

Silastic Hemi Wrist Implant H.p. (Rad.)

Dow Corning Corp. Healthcare Industries Materials, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K812053 is the FDA 510(k) clearance record for SILASTIC HEMI WRIST IMPLANT H.P. (RAD.), a class II device, cleared for Dow Corning Corp. Healthcare Industries Materials on under FDA product code KXE (Prosthesis, Wrist, Hemi-, Ulnar). FDA records list 31 510(k) clearances for Dow Corning Corp. Healthcare Industries Materials, from to . As of , FDA records show no recalls naming K812053.

Clearance record

Decision date
Received
(28 days to decision)
Product code
KXE Prosthesis, Wrist, Hemi-, Ulnar
Regulation
21 CFR 888.3810
Device class
Class II
Review panel
Orthopedic
Applicant
Dow Corning Corp. Healthcare Industries Materials 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KXE

Trailing 12 months

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

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