510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K192294Substantially Equivalent

I Do

I do Biotech Co., Ltd., Daegu, KR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K192294 is the FDA 510(k) clearance record for I Do, a class II device, cleared for I DO Biotech Co., Ltd. on under FDA product code DZE (Implant, Endosseous, Root-Form). FDA records list one 510(k) clearance for I DO Biotech Co., Ltd. As of , FDA records show no recalls naming K192294.

Clearance record

Decision date
Received
(343 days to decision)
Product code
DZE Implant, Endosseous, Root-Form
Regulation
21 CFR 872.3640
Device class
Class II
Review panel
Dental
Applicant
I DO Biotech Co., Ltd. #C, 135, Seongseodong-Ro, Dalsoe-Gu, Daegu, KR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DZE

Trailing 12 months
19 clearances under product code DZE in the twelve months to October 2026, December 2025 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code DZE, trailing twelve months
MonthClearances
November 20251
December 20254
January 20261
February 20262
March 20264
April 20260
May 20261
June 20264
July 20260
August 20261
September 20261
October 20260