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Scott's Premium German Ridge Mapping Implant Calipers

FDA UDI

Class I (US FDA UDI)

by Scott's Dental Supply L.l.c.

Identity

Trade Name
SCOTT'S PREMIUM GERMAN RIDGE MAPPING IMPLANT CALIPERS FDA UDI
Generic Name
Facebow FDA UDI
Device Name
SCOTT'S PREMIUM GERMAN RIDGE MAPPING IMPLANT CALIPERS FDA UDI
Model / Reference
190-RMC FDA UDI
Description
SCOTT'S PREMIUM GERMAN RIDGE MAPPING IMPLANT CALIPERS FDA UDI

Identifiers

Catalog Number
190-RMC FDA UDI
Primary DI / UDI-DI
D778190RMC0 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Facebow FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Facebow

Scott's Premium German Ridge Mapping Implant Calipers by Scott's Dental Supply L.l.c. — 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

Sources (1)

  • FDA UDI b6ec701c-1d31-4d25-865c-5919b4934676 35 fields · synced Jun 1, 2026