510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K161335Substantially Equivalent

Dual Top Screw System

Jeil Medical Corporation, Seoul, KR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K161335 is the FDA 510(k) clearance record for Dual Top Screw System, a class II device, cleared for Jeil Medical Corporation on under FDA product code OAT (Implant, Endosseous, Orthodontic). FDA's definition for product code OAT reads: "It is intended to provide a fixed anchorage point for attachment of orthodontic appliances to facilitate the orthodontic movement of teeth. It is used temporarily and is removed after orthodontic treatment has been completed". FDA records list 53 510(k) clearances for Jeil Medical Corporation, from to . As of , FDA records show no recalls naming K161335.

Clearance record

Decision date
Received
(287 days to decision)
Product code
OAT Implant, Endosseous, Orthodontic
Regulation
21 CFR 872.3640
Device class
Class II
Review panel
Dental
Applicant
Jeil Medical Corporation 702, 703, 704, 705, 706, 804, 805,807,812-Ho ,55,, Seoul, KR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OAT

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