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Explor

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
EXPLOR FDA UDI
Generic Name
Elbow radius prosthesis FDA UDI
Model / Reference
11-210023 FDA UDI

Identifiers

Catalog Number
11-210023 FDA UDI
Primary DI / UDI-DI
00880304210325 FDA UDI
510(k) Number
K040611 FDA UDI
K051385 FDA UDI
FDA Product Code
KWI FDA UDI
GMDN Term
Elbow radius prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3170 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

No

FDA UDI

Category: Elbow radius prosthesis

Explor by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Elbow radius prosthesis.

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 0642d8c4-549b-4a2a-8828-11f197ae758c 36 fields · synced May 30, 2026