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Toegrip® Classic

FDA UDI

Class II (US FDA UDI)

by Tyber Medical

Identity

Trade Name
TOEGRIP® CLASSIC FDA UDI
Generic Name
Phalangeal joint arthrodesis implant FDA UDI
Device Name
ToeGrip Classic Small 10° FDA UDI
Model / Reference
TGSS10 FDA UDI
Description
ToeGrip Classic Small 10° FDA UDI

Identifiers

Primary DI / UDI-DI
00196449035823 FDA UDI
510(k) Number
K133477 FDA UDI
FDA Product Code
HTY FDA UDI
GMDN Term
Phalangeal joint arthrodesis implant 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

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
MRI Safety
MR Safe FDA UDI

Category: Phalangeal joint arthrodesis implant

Toegrip® Classic by Tyber Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phalangeal joint arthrodesis implant.

Cleared under the same submission

K133477 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tyber Medical

Sources (1)

  • FDA UDI 8d604930-fd6f-46e2-919c-4ea70a7e1df6 35 fields · synced May 30, 2026