← Back to catalogue

OrthoButton AL

FDA UDI

Class II (US FDA UDI)

by Riverpoint Medical Llc

Identity

Trade Name
OrthoButton AL FDA UDI
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name
Soft tissue fixation device FDA UDI
Model / Reference
RP-OBAL-80 FDA UDI
Description
Soft tissue fixation device FDA UDI

Identifiers

Primary DI / UDI-DI
00812444026986 FDA UDI
FDA Product Code
MBI FDA UDI
GMDN Term
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

No

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: Tendon/ligament bone anchor, non-bioabsorbable

OrthoButton AL by Riverpoint Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament bone anchor, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d28e6565-e56b-46a7-b6a0-b4f6e6a433d0 33 fields · synced May 30, 2026