510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K872490Substantially Equivalent

1.1 Screwdrivers

Micro-Aire Surgical Instruments, Inc., San Fernando CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K872490 is the FDA 510(k) clearance record for 1.1 SCREWDRIVERS, a class I device, cleared for Micro-Aire Surgical Instruments, Inc. on under FDA product code LRZ (Screwdriver, Surgical). FDA records list 40 510(k) clearances for Micro-Aire Surgical Instruments, Inc., from to . As of , FDA records show no recalls naming K872490.

Clearance record

Decision date
Received
(30 days to decision)
Product code
LRZ Screwdriver, Surgical
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Micro-Aire Surgical Instruments, Inc. 505 Fourth St., San Fernando CA
Third party review
No

Clearances, product code LRZ

Trailing 12 months

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

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