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RingLoc® Hip System

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
RingLoc® Hip System FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Model / Reference
103537 FDA UDI

Identifiers

Catalog Number
103537 FDA UDI
Primary DI / UDI-DI
00880304185715 FDA UDI
510(k) Number
K082446 FDA UDI
K912245 FDA UDI
K971890 FDA UDI
K990032 FDA UDI
K991807 FDA UDI
FDA Product Code
JDI FDA UDI
LPH FDA UDI
KWA FDA UDI
JWH FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 FDA UDI
888.3358 FDA UDI
888.3330 FDA UDI
888.3560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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: Orthopaedic bone screw, non-bioabsorbable, sterile

RingLoc® Hip System by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw, non-bioabsorbable, sterile.

Cleared under the same submission

K082446 also covers:

K912245 also covers:

K971890 also covers:

K990032 also covers:

K991807 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet Orthopedics, Inc.

Sources (1)

  • FDA UDI 96d4aef6-c649-4ceb-a2a3-c6dcc4b7627a 36 fields · synced May 30, 2026