Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
2033784903
Device Listing 2033784903
Listing Summary
#
Listing key
2033784903
Premarket submission
K102305
Device
HASS ZIRTOOTH MODEL ZORTOOTH H. ZIRTOOTH T. ZIRTOOTHC, ZIRTOOTH P
Applicant
Hass Corp.
Product code
EIH
Decision date
2010-12-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
124407
3008754429
3008754429
HASS CORP.
1
N
2026-01-01
77-14, Gwahakdanji-ro Gangneung-si Gangwon KR 25452