← Back to catalogue

MIS BondBone

FDA UDI

Class II (US FDA UDI)

by MIS Implants Technologies Ltd.

Identity

Trade Name
MIS BondBone FDA UDI
Generic Name
Synthetic bone graft FDA UDI
Device Name
BondBone 1cc Bonding-Graft Material FDA UDI
Model / Reference
BS-BB010 FDA UDI
Description
BondBone 1cc Bonding-Graft Material FDA UDI

Identifiers

Primary DI / UDI-DI
07290108990065 FDA UDI
FDA Product Code
LYC FDA UDI
GMDN Term
Synthetic bone graft 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

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

Category: Synthetic bone graft

MIS BondBone by MIS Implants Technologies Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic bone graft.

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

Sources (1)

  • FDA UDI be59a365-7681-42fe-b55a-f5e07c89a1c4 33 fields · synced Jun 1, 2026