Manufacturer registered with FDA
Daekwang Idm
Joong-gu, South Korea. Lists 3 dental device types with FDA across 1 registered establishment.
- Device types listed
- 3
- Brands and models
- 4
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1South Korea
Devices listed with FDA
What Daekwang Idm currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Endosseous Dental Implant AbutmentNHA · Class 2 | Implant abutments | Maker | Abutment, implant, dental, endosseousIMPLANT, ENDOSSEOUS, ROOT-FORMAbutment, implant, dental, endosseous | 2017 |
| Root-Form Endosseous ImplantDZE · Class 2 | Dental implants | Maker | IMPLANT, ENDOSSEOUS, ROOT-FORMAbutment, implant, dental, endosseous | 2018 |
| Dental Instrument HandleEJB · Class 1 | Dental hand instruments | Maker | HANDLE, INSTRUMENT, DENTAL | 2018 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Also lists devices cleared under other names
Daekwang Idm lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: LK Consulting Group USA, Inc. (1), KJ Meditech Co., Ltd. (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 21 Mar 2014 | K132144 | KERATOR | LK Consulting Group USA, Inc. | DZE Root-Form Endosseous Implant |
| 8 Aug 2012 | K112787 | KERATOR | KJ Meditech Co., Ltd. | NHA Endosseous Dental Implant Abutment |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| DAEKWANG I.D.MFDA reg. 3009528826 | Seoul, South Korea | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10053764). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.