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Endopearl

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
ENDOPEARL FDA UDI
Generic Name
Tendon/ligament bone anchor, bioabsorbable FDA UDI
Device Name
ENDOPEARL 7MM, SOFT TISSUE FIXATION DEVICE FDA UDI
Model / Reference
C8057 FDA UDI
Description
ENDOPEARL 7MM, SOFT TISSUE FIXATION DEVICE FDA UDI

Identifiers

Catalog Number
C8057 FDA UDI
Primary DI / UDI-DI
20845854014292 FDA UDI
510(k) Number
K984171 FDA UDI
FDA Product Code
MAI FDA UDI
GMDN Term
Tendon/ligament bone anchor, bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 7 Millimeter FDA UDI

Category: Tendon/ligament bone anchor, bioabsorbable

Endopearl by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament bone anchor, bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 303527a1-fc35-475c-aaf4-72c7130b2dd0 38 fields · synced May 30, 2026