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RegenaVate™ Formable DBM RT, 2cc

FDA UDI

Class II (US FDA UDI)

by Rti Surgical, Inc.

Identity

Trade Name
RegenaVate™ Formable DBM RT, 2cc FDA UDI
Generic Name
Bone matrix implant, human-derived FDA UDI
Device Name
Formable DBM RT, 2cc FDA UDI
Model / Reference
ZR0202 FDA UDI
Description
Formable DBM RT, 2cc FDA UDI

Identifiers

Catalog Number
005302Z FDA UDI
Primary DI / UDI-DI
00854095006771 FDA UDI
510(k) Number
K080418 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

Yes

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bone matrix implant, human-derived

RegenaVate™ Formable DBM RT, 2cc by Rti Surgical, Inc. — 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

Manufacturer
Rti Surgical, Inc.

Sources (1)

  • FDA UDI 3e475e78-f021-4ba5-a8bb-dcb8f5a72275 36 fields · synced May 30, 2026