Data / Medical devices / South Korea / Hass Corp.
Hass Corp.: FDA-registered device maker in Gangneung-si Gangwon, South Korea, 3 510(k) clearances
Hass Corp. is registered with the FDA (registration 3025604798) in Gangneung-si Gangwon, South Korea. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated June 11, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3025604798
- Address
- 103, Gwahakdanji-Ro, Gangneung-si Gangwon, South Korea, 25452
- Owner or operator
- HASS CORP. (10034719)
- Roles
- Manufacturer
- First device listed
- October 24, 2011
- Registered through
- 2026
- Brand names listed
- Amber LiSi-POM Series, Amber LiSi-POZ Series, Amber Mill Meso, Amber Mill Q Series & Amber Mill Direct Series, Amber Mill Series, Amber Press Master, Amber Press Series, Rosetta SM and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Crown, Preformed | ELZ | 1 | Manufacturer | accessdata.fda.gov |
| Powder, Porcelain | EIH | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 11, 2026 | K260859 | Rosetta SM, Rosetta SP | EIH | Substantially Equivalent | Hass Corp. | accessdata.fda.gov |
| August 26, 2021 | K202952 | Amber Mill Q Series & Amber Mill Direct Series | EIH | Substantially Equivalent | Hass Corp. | accessdata.fda.gov |
| July 14, 2016 | K160102 | Amber Mill Series and Amber Press Series | EIH | Substantially Equivalent | Hass Corp. | accessdata.fda.gov |
Compare with other makers
Updated June 11, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.