FDA UDI In Commercial Distribution 🇺🇸 United States

SECULOK™ ACP SYSTEM

DI: 08800247357545 · Model: FCA1033 · CG MedTech Co.,Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SECULOK™ ACP SYSTEM
Primary DI
08800247357545
Version / Model
FCA1033
Company Name
CG MedTech Co.,Ltd.
Labeler DUNS
688811082
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-31
Public Version
1
Public Version Date
2026-04-08
Public Version Status
New
Public Device Record Key
409f9f1a-1bae-4e6e-a2ca-27a27b9abc34

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWQ Appliance, fixation, spinal intervertebral body

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 08800247357545

Premarket Submissions

Submission Number Supplement Number
K182055 000