Hdx Will Corp.
Active in EUDAMEDSouth Koreafrom SRN EUDAMED FDA SRN KR-MF-000019877 FEI 3013511605
Hdx Will Corp. is a medical device manufacturer based in South Korea, with 26 devices listed in FDA GUDID, FDA 510(k) and EUDAMED (FDA Class II; EU Class IIa) as of 14 Nov 2026.
- Devices
- 26
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 19
- FDA 510(k) 6
- EUDAMED 3
- Device classes
- FDA Class II 24
- EU Class IIa 2
- Top EMDN categories
- Sites and related companies
- KTR Europe GmbH authorised representative
- Identifiers
- EUDAMED SRN KR-MF-000019877
- FDA FEI 3013511605
- DUNS 689605054
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI
- Authorised rep.
- KTR Europe GmbHDE
What Hdx Will Corp. makes
HDX Will Corp. manufactures digital dental X-ray systems, including stationary panoramic/tomographic and intraoral units, as well as hand-held intraoral models. Their portfolio also includes intraoral optical scanning systems and specialized software for dental imaging, such as general-purpose X-ray application software and radiological picture archiving and communication systems (PACS).
The company’s devices are classified as Class II or Class IIa under global regulatory frameworks, with listings in the EU’s eudamed registry, the FDA’s 510(k) and UDI databases. The manufacturer is based in South Korea.
Catalogue
Search and filter all 26 devicesCompany details
- EUDAMED SRN
- KR-MF-000019877
- FDA FEI number
- 3013511605
- DUNS number
- 689605054
- EUDAMED status
- Active
- EUDAMED registered name
- HDX WILL Corp.
- EUDAMED abbreviated name
- HDX WILL
- Registered address
- 38, Osongsaengmyeong 4-ro, Osong-eup, Heungdeok-gu, 28161, Cheongju-si, Chungcheongbuk-do, South Korea
- Website
- www.hdxwill.co.kr
- global@hdx.co.kr
- Phone
- +82-2-1588-2754
- PRRC contact
- Dong-Hun Jeong
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 30 Jun 2031
TÜV Rheinland LGA Products GmbH 0197 1 certificate
- HZ 2126571-1 Active
Quality management system EU MDR
- Issued
- 1 Jul 2026
- Expires
- 30 Jun 2031
Frequently asked questions
How many devices does HDX WILL CORP. have in the registry?
The registry currently lists 26 devices for HDX WILL CORP.. Devices recorded under merged duplicate company entries are counted once.
Which registries list HDX WILL CORP.'s devices?
Among its 26 most recently registered devices, HDX WILL CORP. has devices listed in EUDAMED (3 devices), FDA 510(k) (6 devices) and FDA GUDID (19 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do HDX WILL CORP.'s devices fall under?
Among its 26 most recently registered devices, the classes recorded for HDX WILL CORP.'s devices are Class IIa and Class II. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for HDX WILL CORP.?
EUDAMED lists 1 certificate for HDX WILL CORP. (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 1 Jul 2026.
What are the newest devices from HDX WILL CORP. in the registry?
The most recently registered devices listed for HDX WILL CORP. include WillCeph Pro, Xcam, DENTRI Max DENTRI-Sα and DENTRIα Series.