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GEO Hammertoe Screw

FDA UDI

Class II (US FDA UDI)

by Gramercy Extremity Orthopedics, Llc.

Identity

Trade Name
GEO Hammertoe Screw FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Device Name
Hammertoe Screw 2.5x13 Solid 0 Deg. Ti FDA UDI
Model / Reference
15002513 FDA UDI
Description
Hammertoe Screw 2.5x13 Solid 0 Deg. Ti FDA UDI

Identifiers

Primary DI / UDI-DI
B471150025130 FDA UDI
510(k) Number
K170571 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, sterile 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

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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 13 Millimeter FDA UDI
Outer Diameter — 2.5 Millimeter FDA UDI

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

GEO Hammertoe Screw by Gramercy Extremity Orthopedics, Llc. — 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

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Manufacturer

Sources (1)

  • FDA UDI 304660f3-7399-42ad-856d-9700db20c438 37 fields · synced May 31, 2026