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Ring-Lok

FDA UDI

Class II (US FDA UDI)

by Implants International Ltd

Identity

Trade Name
RING-LOK FDA UDI
Generic Name
Metallic femoral head prosthesis FDA UDI
Device Name
Modular Bi-Polar 59mm Dia. (28mm Head) For Uncemented Applications FDA UDI
Model / Reference
Modular Bi-Polar (59mm- 28mm Head) FDA UDI
Description
Modular Bi-Polar 59mm Dia. (28mm Head) For Uncemented Applications FDA UDI

Identifiers

Catalog Number
BP2395 FDA UDI
Primary DI / UDI-DI
05051693307858 FDA UDI
510(k) Number
K132539 FDA UDI
FDA Product Code
KWY FDA UDI
GMDN Term
Metallic femoral head prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3390 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 59 Millimeter FDA UDI

Category: Metallic femoral head prosthesis

Ring-Lok by Implants International Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic femoral head 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 a0e82959-4194-4d5e-b622-acf71bf65726 38 fields · synced Jun 8, 2026