FDA UDI In Commercial Distribution 🇺🇸 United States

ReActive® Implant

DI: 10841307103646 · Model: 754210 · IMPLANT DIRECT SYBRON MANUFACTURING LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ReActive® Implant
Primary DI
10841307103646
Version / Model
754210
Catalog Number
754210
Company Name
IMPLANT DIRECT SYBRON MANUFACTURING LLC
Labeler DUNS
868856969
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
b34eb131-5056-4973-ac6a-84e174e07d59

Device Description

4.2mmD x 10mmL, 3.5mmD Platform

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DZE Implant, Endosseous, Root-Form

GMDN Terms

Code Name
55847 Dental implant system

Identifiers

Type ID
Primary 10841307103646

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K090234 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 4.2mmD x 10mmL