Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008922120

FEI Number

3008922120

Entity Name

SHERPA KOREA

City/State/Country

Saha-gu Busan, KR

Establishment Address

438-1, Hasinbeonyeong-ro, Saha-gu Busan 49301, KR

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device

Owner / Operator

Sherpa (Owner Number: 10035326)

Owner / Operator Contact Address

#902, 468, Gangseo-ro, Gangseo-gu, KR-11 07573, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Deli-Temp SP Reline Soft e&e Denture Soft Reline Kit e&e Putty Fast Set DIOSIL Heavy Body DIOSIL Bite Delikit Medium Body Precisil Bite Registration Hard Precisil Mask Precisil Light Body FS Precisil Secret Vaccusil Bite Registration Vaccusil Heavy Body FS Deli Mask Delikit Bite Registration Precisil Heavy Body FS Delikit Heavy Body FS Precisil Light Body Precisil Regular Body FS Precisil Tornado Monophase Delikit Tornado Heavy Body Precisil Putty FS Vaccusil Light Body Delikit Regular Body FS Precisil Plant Light Body Deli Plant Light Body Precisil Heavy Body Delikit Extra Light Body Precisil Heavy Body Hybrid set Deli plant Light Body FS Imflex Monophase Mojo Complete STRONGBITE PLUS REGULAR BODY Deli Plant Heavy Body FS Precisil Extra Light Body Imflex Light Body Fast Delikit Heavy Body Precisil Jumbo Monophase Precisil Regular Body Biggg Densurefit Delikit Putty RS Precisil Bite Registration Trimming Precisil Plant Heavy Body Delikit Light Body FS Precisil Bite Registration Fast Precisil Light Body Trend Delikit Putty FS Precisil Bite Registration Normal Precisil Medium Body Delikit Light Body Precisil Bite Registration Imflex Heavy Body Delikit Regular Body Precisil Plant Heavy Body FS Delikit Jumbo Monophase Precisil Big Precisil Putty RS Vaccusil Light Body FS Deli Plant Heavy Body Precisil Denture Deli-Big Precisil Heavy Body Biggg Delikit Tornado Monophase Vaccusil Heavy Body FS 120ml Precisil Tornado Heavy Body Imflex Light Body Precisil Light Body Hybrid set Precisil Soft Imflex Putty Imflex Heavy Body Fast Precisil Regular Body STRONGBITE PLUS PUTTY Deli-Border Vaccusil Heavy Body Delikit Secret Precisil Premium Light Body Vaccusil Heavy Body RS 120ml Deli Denture Jackpot Light Body Imflex Putty Fast Imflex Bite STRONGBITE PLUS BITE REGISTRATION Bio Cell Light Body Bio Cell Heavy Body Jackpot Light Body Fast Bio Cell Bite Deli-Bite Clear Precisil Jumbo Big STRONGBITE PLUS LIGHT BODY Fast Set STRONGBITE PLUS HEAVY BODY Fast Set Monophase Simplify Precisil Bite Trimming Delikit Premium Putty Jackpot Big Light Body fast Delikit Premium Light Body Jackpot Bite Neo Fit Light Body 3 Delikit 200 Heavy Body e&e putty eco e and e putty Neo Fit Heavy Body Neo Fit Light Body e&e Putty Eco Regular Set DIOSIL Putty DIOSIL Light body e&e Bite Registration Excel Impression Tray Green Flat Tip 6.5 mm Yellow Mixing Tip 4.5 mm

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EBG	Crown And Bridge, Temporary, Resin	Dental	Class 2	872.3770	2012-03-12
EBP	Reliner, Denture, Over The Counter	Dental	Class 2	872.3560	2023-12-07
ELW	Material, Impression	Dental	Class 2	872.3660	2011-02-21
EHY	Tray, Impression, Preformed	Dental	Class 1	872.6880	2011-10-24
EID	Syringe, Restorative And Impression Material	Dental	Class 1	872.4565	2025-02-03

Official Correspondent

HyeongJoo Moon

US Agent Details

Grace Kim Email: gracejschem@hotmail.com Phone: (310) 5983012

Related Public Records

Same Entity

Sherpa

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K952614	Dentsply Intl.	JELTRATE PLUS ANTIMICROBIAL IMPR. MATERIAL	1996-08-13

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3007210751	DENTSCARE LTDA	Joinville Santa Catarina, BR
1410097	GC AMERICA INC.	ALSIP, IL, US
3015396763	MGNEWTON LTD.	Gyengsan-si Gyeongbuk, KR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008922120. Last updated year: 2026. Please use registration number 3008922120 when referencing this establishment in official correspondence.