510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K921167Substantially Equivalent

Ultrablade

Micron Technology, Inc., Boulder CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K921167 is the FDA 510(k) clearance record for ULTRABLADE, a class I device, cleared for Micron Technology, Inc. on under FDA product code GDX (Scalpel, One-Piece). FDA records list 2 510(k) clearances for Micron Technology, Inc., from to . As of , FDA records show no recalls naming K921167.

Clearance record

Decision date
Received
(141 days to decision)
Product code
GDX Scalpel, One-Piece
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Micron Technology, Inc. Centennial Creek Office Park, Boulder CO
510(k) summary
Statement
Third party review
No

Clearances, product code GDX

Trailing 12 months

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

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