FDA UDI In Commercial Distribution 🇺🇸 United States

Slidematic Facebow

DI: D04020001121 · Model: 200011-2 · WHIP-MIX CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Slidematic Facebow
Primary DI
D04020001121
Version / Model
200011-2
Catalog Number
200011-2
Company Name
WHIP-MIX CORPORATION
Labeler DUNS
006385173
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-22
Public Version
2
Public Version Date
2025-09-12
Public Version Status
Update
Public Device Record Key
d2c733a1-b3f8-43bd-a25a-4b6de4f049c0

Device Description

A facebow is a device intended for use in a dental diagnostic procedure to record the relative position of the mandible to the temporomandibular joints (TMJs) and/or to record the spatial relationship between the maxilla and mandible. This is a reusable device.

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
Yes
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
No

Product Codes

Code Name
KCR Facebow

GMDN Terms

Code Name
35700 Facebow

Identifiers

Type ID
Primary D04020001121