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Quick mount Facebow

FDA UDI

Class II (US FDA UDI)

by Whip-Mix Corp.

Identity

Trade Name
Quick mount Facebow FDA UDI
Generic Name
Facebow FDA UDI
Device Name
#8645 QUICK MOUNT FACE BOW W/SCREWS FDA UDI
Model / Reference
15911 FDA UDI
Description
#8645 QUICK MOUNT FACE BOW W/SCREWS FDA UDI

Identifiers

Primary DI / UDI-DI
D040159110 FDA UDI
FDA Product Code
KRC FDA UDI
GMDN Term
Facebow FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Facebow

Quick mount Facebow by Whip-Mix Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Facebow.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Whip-Mix Corp.

Sources (1)

  • FDA UDI 69c46444-0edc-4ae9-8bd1-d6bc5e32b7cf 33 fields · synced May 30, 2026