← Back to catalogue

Ponto

FDA UDI

Class II (US FDA UDI)

by Oticon Medical

Identity

Trade Name
Ponto FDA UDI
Generic Name
Craniofacial bone screw, non-bioabsorbable FDA UDI
Device Name
Wide implant, 3 mm, with abutment, 6 mm FDA UDI
Model / Reference
M51140 FDA UDI
Description
Wide implant, 3 mm, with abutment, 6 mm FDA UDI

Identifiers

Catalog Number
M51140 FDA UDI
Primary DI / UDI-DI
05712149003952 FDA UDI
FDA Product Code
MAH FDA UDI
GMDN Term
Craniofacial bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3302 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 4.5 Millimeter FDA UDI
Length — 6 Millimeter FDA UDI
Length — 3 Millimeter FDA UDI

Category: Craniofacial bone screw, non-bioabsorbable

Ponto by Oticon Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Craniofacial bone screw, non-bioabsorbable.

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
Oticon Medical

Sources (1)

  • FDA UDI 0c5719b5-b703-435f-839d-eb9c31b61bdc 36 fields · synced Jun 1, 2026