FDA UDI In Commercial Distribution 🇺🇸 United States

Foundation Surgical Interwedge

DI: 00810141040762 · Model: FS50-355000 · FOUNDATION SURGICAL GROUP INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Foundation Surgical Interwedge
Primary DI
00810141040762
Version / Model
FS50-355000
Catalog Number
FS50-355000
Company Name
FOUNDATION SURGICAL GROUP INC
Labeler DUNS
119029419
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-24
Public Version
1
Public Version Date
2025-11-03
Public Version Status
New
Public Device Record Key
a55f48c2-afde-4e7c-98b0-e505a8b90523

Device Description

Cover Plate Remover

Device Characteristics

Single Use
No
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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 00810141040762

Customer Contacts

Phone
727-209-7436

Premarket Submissions

Submission Number Supplement Number
K241487 000