FDA.reportPublic FDA data

Bone Foam

Primary DI
00810075280999
Brand
Bone Foam
Company
BONE FOAM, INC.
Model
10-910-02-C
Catalog number
10-910-02-C
Device description
Head Cradle - Coated - Box of 4
Published
2022-05-22
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
CCXSupport, Patient Position
EPWSupport, head, surgical, ENT

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
CCXSupport, Patient PositionAnesthesiology1
EPWSupport, Head, Surgical, EntGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810075280036PrimaryGS10
00810075280999Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810075280036008100752800368100752800360810075280036
00810075280999008100752809998100752809990810075280999

GMDN Terms#

Term, Definition table
TermDefinition
Freestanding patient positioner, reusableA preformed patient-contact device (e.g., cushion, pad, bolster, wedge, elevation pillow) designed to be placed freely on a flat surface (e.g., operating table, stretcher) to position and stabilize a patient or body part typically in preparation for and during various medical procedures [e.g., to align the head, neck and thorax to optimise laryngoscopy in anaesthesia]; it is not attached to a parent device. It is made of shock-absorbing materials (e.g., memory foam) to reduce pressure on the bony prominences of a body part (e.g., torso, arm, leg), and some types are inflatable to provide variable support (e.g., to level the spine in a lateral position). This is a reusable device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
079636174
Device count
4
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810075281675BoneFoam104.UPC-SUK-BX5104.UPC-SUK-BX52026-07-28
00810075281668BoneFoam104.NPC-SUK-BX5104.NPC-SUK-BX52026-06-12
00810075280005BoneFoam10-910-0010-910-002022-05-22
00810075280067BoneFoam10-910-0310-910-032022-05-22
00810075281316BoneFoam925.UPS-DBC-BX20925.UPS-DBC-BX202022-12-19
00810075281279BoneFoam925.UPS-R-UB925.UPS-R-UB2022-11-21
00810075281286BoneFoam925.UPS-R-LB925.UPS-R-LB2022-11-21
00810075281293BoneFoam925.UPS-S-UB925.UPS-S-UB2022-11-21
00810075281309BoneFoam925.UPS-S-LB925.UPS-S-LB2022-11-21
00810075281347BoneFoam925.UPS-R925.UPS-R2022-11-21
00810075281354BoneFoam925.UPS-S925.UPS-S2022-11-21
00810075280074BoneFoam10-910-06-C10-910-06-C2022-05-22
00810075280081BoneFoam10-910-01-C10-910-01-C2022-05-22
00810075281521BoneFoam104.NPL-SUK-BX5104.NPL-SUK-BX52025-08-15
00810075281606BoneFoam925.SG-BX10925.SG-BX102025-08-15
00810075281620BoneFoam925.ZDK-DOC-BX12925.ZDK-DOC-BX122025-08-15
00810075281491BoneFoam104.NPL104.NPL2025-08-15
00810075281507BoneFoam104.NPLB104.NPLB2025-08-15
00810075281514BoneFoam104.NPL-SUK-BX5104.NPL-SUK-BX52025-08-15
00810075281538BoneFoam104.NPSB104.NPSB2025-08-15

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Primary DI, Brand, Company table
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00811836030907TrenGuard™Dan Allen Surgical LLCCCX2026-06-26
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00814247021304Panniculus Retraction KitCLINICAL INNOVATIONS, LLCCCX2026-05-31
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10080196413737MEDLINEMEDLINE INDUSTRIES, INC.CCX2026-04-27
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