FDA UDI In Commercial Distribution 🇺🇸 United States

Lynx Pro

DI: D950131840 · Model: 500 Mini 4H Non-Fiber-Optic · LARES RESEARCH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Lynx Pro
Primary DI
D950131840
Version / Model
500 Mini 4H Non-Fiber-Optic
Catalog Number
13184
Company Name
LARES RESEARCH
Labeler DUNS
009127838
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-18
Public Version
1
Public Version Date
2024-10-28
Public Version Status
New
Public Device Record Key
e4df9ee1-e5c5-420d-93dd-9bffbd1ee77c

Device Description

Lynx Pro 550 Handpiece Push button Mini head 4H Non-Fiber-Optic

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
Yes
Has Lot/Batch Number
No
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
EFB Handpiece, Air-Powered, Dental

GMDN Terms

Code Name
66244 Dental surgical power tool motorized handpiece/set, pneumatic

Identifiers

Type ID
Primary D950131840

Customer Contacts

Phone
5303451767

Premarket Submissions

Submission Number Supplement Number
K141221 000