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Unit-Assy Slidematic

FDA UDI

Class I (US FDA UDI)

by Whip-Mix Corp.

Identity

Trade Name
Unit-Assy Slidematic FDA UDI
Generic Name
Facebow FDA UDI
Device Name
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. CLOSE FDA UDI
Model / Reference
20002950 FDA UDI
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. CLOSE FDA UDI

Identifiers

Primary DI / UDI-DI
D04020002950 FDA UDI
FDA Product Code
KCR FDA UDI
GMDN Term
Facebow FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3220 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

Unit-Assy Slidematic by Whip-Mix Corp. — Class I — 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 5a3d213e-743c-4997-9baa-34033b595762 33 fields · synced May 31, 2026