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BoneFoam

FDA UDI

Class I (US FDA UDI)

by Bone Foam, Inc.

Identity

Trade Name
BoneFoam FDA UDI
Generic Name
Freestanding patient positioner, single-use FDA UDI
Device Name
Shin Guard | Box of 10 FDA UDI
Model / Reference
925.SG-BX10 FDA UDI
Description
Shin Guard | Box of 10 FDA UDI

Identifiers

Catalog Number
925.SG-BX10 FDA UDI
Primary DI / UDI-DI
00810075281606 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Freestanding patient positioner, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Freestanding patient positioner, single-use

BoneFoam by Bone Foam, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding patient positioner, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bone Foam, Inc.

Sources (1)

  • FDA UDI 9ec7226e-3d34-421c-97ea-605a87352a92 34 fields · synced Jun 1, 2026