← Back to catalogue

Exactech

FDA UDI

Class II (US FDA UDI)

by Exactech, Inc.

Identity

Trade Name
Exactech FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Model / Reference
120-65-30 FDA UDI

Identifiers

Catalog Number
120-65-30 FDA UDI
Primary DI / UDI-DI
10885862019868 FDA UDI
510(k) Number
K993082 FDA UDI
FDA Product Code
LPH FDA UDI
JDI FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3350 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 30 Millimeter FDA UDI
Outer Diameter — 6.5 Millimeter FDA UDI

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

Exactech by Exactech, 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

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

Manufacturer
Exactech, Inc.

Sources (1)

  • FDA UDI ac08045d-41c3-4316-80e2-896ba2b6d5e0 35 fields · synced May 30, 2026