FDA UDI In Commercial Distribution 🇺🇸 United States

Lantern

DI: 00810832032069 · Model: 403544 · Orthalign, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Lantern
Primary DI
00810832032069
Version / Model
403544
Catalog Number
403544
Company Name
Orthalign, Inc.
Labeler DUNS
023266163
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-13
Public Version
1
Public Version Date
2024-12-23
Public Version Status
New
Public Device Record Key
3a02012b-ca92-40fa-bdd4-f37e0511b8e5

Device Description

Adapter Clip, 17.6mm

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
ONN Intraoperative Orthopedic Joint Assessment Aid

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 00810832032069

Customer Contacts

Phone
866-582-0879

Premarket Submissions

Submission Number Supplement Number
K242616 000