← Back to catalogue

JMA Optic

FDA UDI

Class I (US FDA UDI)

by zebris MEDICAL GmbH

Identity

Trade Name
JMA Optic FDA UDI
Generic Name
Facebow FDA UDI
Device Name
Opto-Electronic Face-Bow for monitoring and tracking of lower jaw movements, USB-Version FDA UDI
Model / Reference
01170011 FDA UDI
Description
Opto-Electronic Face-Bow for monitoring and tracking of lower jaw movements, USB-Version FDA UDI

Identifiers

Catalog Number
NA FDA UDI
Primary DI / UDI-DI
B915011700110 FDA UDI
FDA Product Code
NFS FDA UDI
GMDN Term
Facebow FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.2060 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Facebow

JMA Optic by zebris MEDICAL GmbH — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
zebris MEDICAL GmbH

Sources (1)

  • FDA UDI bb870253-e0f7-4042-aaae-606bf3c225b9 35 fields · synced May 30, 2026