Kj Meditech Co., Ltd. (contract manufacturer, Gwangju, KR): 2 new FDA device listings, incl. abutment, implant, dental, endosseous
Kj Meditech Co., Ltd. (Gwangju): 2 new FDA device listings, incl. abutment, implant, dental, endosseous. Its amount of 2 is above the median of 1 (69th percentile). Dated 106 days ago, it serves as a historical benchmark. Score 55/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 2 · 69th percentile of 2,570 DeviceEstablishmentPulse records · 2.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 116 related KR DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Kj Meditech Co., Ltd. |
| Owner / operator | KJ Meditech Co., Ltd. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Gwangju, KR |
| New listings | 2 |
| Devices | Abutment, Implant, Dental, Endosseous; Implant, Endosseous, Root-Form |
| Product codes | NHA, DZE |
| Device classes | Class II |
| Medical specialties | Dental |
| Brand names | HexaPLUS S OneDrill Implant System |
| First new listing | 2026-07-22 |
| Latest new listing | 2026-07-22 |
| FDA registration number | 3008959419 |
| Registration expires | 2026-12-31 |
| amount percentile | 69th of 2,570 (median 1, 2.0x median) |
| Peer records CSV (117 KR records) | 🔒 Click to unlock → |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-07-22
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (KR first): Zapalign Inc. (foreign exporter, Anyang-si Gyeonggi, KR) · Samsung Medison Co., Ltd. (manufacturer, Gumi-si Gyeongbuk, · Samsung Medison Co., Ltd. (manufacturer, HONGCHEON-GUN Gangw · Osstem Implant Co.,Ltd. (manufacturer, Yeonsu-gu Incheon, KR · Boditech Med Inc. (manufacturer, Chuncheon Gangwon, KR) · Browse all by state and category →
LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Kj Meditech Co., Ltd. and 117 KR peers
- KR DeviceEstablishmentPulse records like this one: 117
- Kj Meditech Co., Ltd.'s amount: 69th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every KR peer: $23,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
55 / 100 Score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
What is the DeviceEstablishmentPulse record for Kj Meditech Co., Ltd. in Gwangju?
Kj Meditech Co., Ltd. (Gwangju, KR), a contract manufacturer, added 2 FDA device listings on 2026-07-22.
How does Kj Meditech Co., Ltd. compare to other DeviceEstablishmentPulse records?
Its amount of 2 sits in the upper half (69th percentile) of 2,570 records; the median is 1. It is 106 days old; check the official source for later updates before acting.
Kj Meditech Co., Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Kj Meditech Co., Ltd. | Gwangju, KR | 2 | 69th | 2026-07-22 |
| Tecomet Inc. | Wilmington, MA | 3 | 77th | 2026-10-15 |
| Bard Shannon Limited | Humacao, PR | 3 | 77th | 2026-10-14 |
| Orchid Orthopedic Solutions Oregon, Inc. | Oregon City, OR | 3 | 77th | 2026-10-05 |
Related records
DeviceEstablishmentPulse: Contract manufacturer DeviceEstablishmentPulse: Foreign establishment
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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.