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Allo-3d-1.0

FDA UDI

Class II (US FDA UDI)

by Salvin Dental Specialties, Llc

Identity

Trade Name
ALLO-3D-1.0 FDA UDI
Generic Name
Bone matrix implant, human-derived FDA UDI
Device Name
1.0cc AlloSculpt-3D Cortical Putty With Chips FDA UDI
Model / Reference
Rev A FDA UDI
Description
1.0cc AlloSculpt-3D Cortical Putty With Chips FDA UDI

Identifiers

Primary DI / UDI-DI
00841336100268 FDA UDI
510(k) Number
K103699 FDA UDI
FDA Product Code
NUN FDA UDI
GMDN Term
Bone matrix implant, human-derived FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3930 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bone matrix implant, human-derived

Allo-3d-1.0 by Salvin Dental Specialties, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone matrix implant, human-derived.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ac938149-e357-44ca-92c1-1c91cb65ed38 34 fields · synced May 30, 2026