510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K130059Substantially Equivalent

Endofast Reliant Scp, Endofast Reliant Lap

Ibi Israel Biomedical Innovations, Ltd., Chalotte NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K130059 is the FDA 510(k) clearance record for ENDOFAST RELIANT SCP, ENDOFAST RELIANT LAP, a class II device, cleared for Ibi Israel Biomedical Innovations , Ltd. on under FDA product code PBQ (Fixation, Non-Absorbable Or Absorbable, For Pelvic Use). FDA's definition for product code PBQ reads: "Attaching suture or stapling ligaments of the pelvic floor". FDA records list one 510(k) clearance for Ibi Israel Biomedical Innovations , Ltd. As of , FDA records show no recalls naming K130059.

Clearance record

Decision date
Received
(200 days to decision)
Product code
PBQ Fixation, Non-Absorbable Or Absorbable, For Pelvic Use
Regulation
21 CFR 884.4530
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Ibi Israel Biomedical Innovations , Ltd. 1914 J.N. Pease Pl., Chalotte NC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PBQ

Trailing 12 months
1 clearance under product code PBQ in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code PBQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260