510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K851719Substantially Equivalent

1070/15 to 1078/17 Various Types Needle Holders

Artiberia, San Antonio TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K851719 is the FDA 510(k) clearance record for 1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS, a class III device, cleared for Artiberia on under FDA product code EZZ (Prosthesis, Vas Deferens). FDA records list 79 510(k) clearances for Artiberia, from to . As of , FDA records show no recalls naming K851719.

Clearance record

Decision date
Received
(68 days to decision)
Product code
EZZ Prosthesis, Vas Deferens
Device class
Class III
Review panel
Unknown
Applicant
Artiberia 4518 Los Ranchitos, San Antonio TX
Third party review
No

Clearances, product code EZZ

Trailing 12 months

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

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