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Cloverleaf Plate 3 holes 2.5/2.8mm Sterile

FDA UDI

Class II (US FDA UDI)

by Biopro, Inc.

Identity

Trade Name
Cloverleaf Plate 3 holes 2.5/2.8mm Sterile FDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Model / Reference
20722 FDA UDI

Identifiers

Primary DI / UDI-DI
M209207220 FDA UDI
510(k) Number
K162674 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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: Orthopaedic fixation plate, non-bioabsorbable

Cloverleaf Plate 3 holes 2.5/2.8mm Sterile by Biopro, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biopro, Inc.

Sources (1)

  • FDA UDI a6a9ec09-a858-448c-83c8-a22fa8547534 33 fields · synced May 30, 2026