510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K134022Substantially Equivalent

Base It

Spident Co., Ltd., Fort Lee NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K134022 is the FDA 510(k) clearance record for BASE IT, a class II device, cleared for Spident Co., Ltd. on under FDA product code EJK (Liner, Cavity, Calcium Hydroxide). FDA records list 18 510(k) clearances for Spident Co., Ltd., from to . As of , FDA records show no recalls naming K134022.

Clearance record

Decision date
Received
(163 days to decision)
Product code
EJK Liner, Cavity, Calcium Hydroxide
Regulation
21 CFR 872.3250
Device class
Class II
Review panel
Dental
Applicant
Spident Co., Ltd. 2115 Linwood Ave., Fort Lee NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EJK

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