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Cmf Visionare

FDA UDI

Class II (US FDA UDI)

by Visionare Llc

Identity

Trade Name
CMF VISIONARE FDA UDI
Generic Name
Craniofacial bone screw, non-bioabsorbable, non-sterile FDA UDI
Device Name
Emergency Self-Tapping Screw D 1.8mm, 11mm FDA UDI
Model / Reference
1.900.137 FDA UDI
Description
Emergency Self-Tapping Screw D 1.8mm, 11mm FDA UDI

Identifiers

Catalog Number
1.900.137 FDA UDI
Primary DI / UDI-DI
10810004515397 FDA UDI
510(k) Number
K180204 FDA UDI
FDA Product Code
DZL FDA UDI
GMDN Term
Craniofacial bone screw, non-bioabsorbable, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4880 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Craniofacial bone screw, non-bioabsorbable, non-sterile

Cmf Visionare by Visionare Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Craniofacial bone screw, non-bioabsorbable, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Visionare Llc

Sources (1)

  • FDA UDI 16c90660-c1da-4345-8da2-1c9be9844afb 36 fields · synced Jun 1, 2026