510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K043358Substantially Equivalent

Reprocessed Ultrasonic Scalpels

Alliance Medical Corp., Phoenix AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K043358 is the FDA 510(k) clearance record for REPROCESSED ULTRASONIC SCALPELS, cleared for Alliance Medical Corp. on under FDA product code NLQ (Single-Use Reprocessed Ultrasonic Surgical Instruments). FDA's definition for product code NLQ reads: "Single-use reprocessed versions of the ultrasonic devices used in surgical procedures either for fragmentation, emulsification and aspiration of soft tissue and hard tissue or for ligation of vessels (under product code “LFL”)...". FDA records list 47 510(k) clearances for Alliance Medical Corp., from to . As of , FDA records show no recalls naming K043358.

Clearance record

Decision date
Received
(182 days to decision)
Product code
NLQ Single-Use Reprocessed Ultrasonic Surgical Instruments
Device class
Unclassified
Review panel
Unknown
Applicant
Alliance Medical Corp. 10232 S. 51st St., Phoenix AZ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NLQ

Trailing 12 months

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

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