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Eagle Suture Anchor 5.5mm Kit

FDA UDI

Class II (US FDA UDI)

by Responsive Orthopedics Llc

Identity

Trade Name
Eagle Suture Anchor 5.5mm Kit FDA UDI
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name
(2) Eagle Screw-in Suture Anchor - 5.5mm (2) Eagle Knotless Suture Anchor - 5.5mm (1) Eagle Drill Guide (1) Eagle Drill 3.5mm (1) Eagle Drill 4.4mm (1) Eagle Tap 5.5mm FDA UDI
Model / Reference
913000-5500 FDA UDI
Description
(2) Eagle Screw-in Suture Anchor - 5.5mm (2) Eagle Knotless Suture Anchor - 5.5mm (1) Eagle Drill Guide (1) Eagle Drill 3.5mm (1) Eagle Drill 4.4mm (1) Eagle Tap 5.5mm FDA UDI

Identifiers

Catalog Number
913000-5500 FDA UDI
Primary DI / UDI-DI
00811714035932 FDA UDI
FDA Product Code
MBI FDA UDI
LXH 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
888.4540 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

Yes

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: Tendon/ligament bone anchor, non-bioabsorbableFluted surgical drill bit, single-useSurgical drill guide, single-useBone tap, single-use

Eagle Suture Anchor 5.5mm Kit by Responsive Orthopedics Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tap, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b3399411-dfd6-4adc-8c89-a92f80c6b462 34 fields · synced May 30, 2026