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Bio-Stinger

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
BIO-STINGER FDA UDI
Generic Name
Meniscus screw FDA UDI
Device Name
BIO-STINGER-V BIOABSORBABLE 10 MM TINTED WITH D&C VIOLET #2, MENISCAL REPAIR DEVICE FDA UDI
Model / Reference
V8210 FDA UDI
Description
BIO-STINGER-V BIOABSORBABLE 10 MM TINTED WITH D&C VIOLET #2, MENISCAL REPAIR DEVICE FDA UDI

Identifiers

Catalog Number
V8210 FDA UDI
Primary DI / UDI-DI
20845854013899 FDA UDI
510(k) Number
K991715 FDA UDI
FDA Product Code
MAI FDA UDI
GMDN Term
Meniscus screw 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

Dimensions & Sizes

Size
Outer Diameter — 10 Millimeter FDA UDI
Length — 10 Millimeter FDA UDI

Category: Meniscus screw

Bio-Stinger by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Meniscus screw.

Cleared under the same submission

K991715 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 53277552-3cc3-4b27-8017-bcfce8716d97 37 fields · synced May 30, 2026