510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K955558Substantially Equivalent

Gip/medi-Globe Sclerotherapy Needles

Medi-Globe GmbH, Tempe AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955558 is the FDA 510(k) clearance record for GIP/MEDI-GLOBE SCLEROTHERAPY NEEDLES, a class II device, cleared for Medi-Globe Corp. on under FDA product code FBK (Endoscopic Injection Needle, Gastroenterology-Urology). FDA's definition for product code FBK reads: "inserted through endoscope for injection of a solution, gas, or implantable materials into gi or gu tissue". FDA records list 26 510(k) clearances for Medi-Globe Corp., from to . As of , FDA records show no recalls naming K955558.

Clearance record

Decision date
Received
(85 days to decision)
Product code
FBK Endoscopic Injection Needle, Gastroenterology-Urology
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Medi-Globe Corp. 6202 S. Maple Ave. # 131, Tempe AZ
510(k) summary
Summary
Third party review
No

Clearances, product code FBK

Trailing 12 months
3 clearances under product code FBK in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FBK, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20261
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260