# SPECLIPSE, INC.

FEI: 3013697074
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: SPECLIPSE, Inc. (#10094634)

Address: #501, #502, #503, #504, #505, 232 Sandan-ro, Danwon-gu, Ansan-si Gyeonggi, 15433, KR



## Products

Total registered: 1
Top product codes: GEX
Regulation §: 878.4810

Proprietary names: PICOFY, PICO-K

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223013697074%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3013697074