510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K884558Substantially Equivalent

Iop Adjustable Stirrup

Mend Technologies, Inc., Dallas TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K884558 is the FDA 510(k) clearance record for IOP ADJUSTABLE STIRRUP, a class I device, cleared for Mend Technologies, Inc. on under FDA product code BWN (Table And Attachments, Operating-Room). FDA records list 3 510(k) clearances for Mend Technologies, Inc., from to . As of , FDA records show no recalls naming K884558.

Clearance record

Decision date
Received
(17 days to decision)
Product code
BWN Table And Attachments, Operating-Room
Regulation
21 CFR 878.4950
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Mend Technologies, Inc. 5757 Alpha Rd., Dallas TX
Third party review
No

Clearances, product code BWN

Trailing 12 months

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

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