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GRYPHON Flex

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
GRYPHON Flex FDA UDI
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name
GRYPHON Flex Knotless PEEK Anchor PEEK Anchor STRAIGHT FDA UDI
Model / Reference
208955 FDA UDI
Description
GRYPHON Flex Knotless PEEK Anchor PEEK Anchor STRAIGHT FDA UDI

Identifiers

Catalog Number
208955 FDA UDI
Primary DI / UDI-DI
10886705032488 FDA UDI
510(k) Number
K232492 FDA UDI
FDA Product Code
MBI FDA UDI
GMDN Term
Tendon/ligament bone anchor, non-bioabsorbable 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: Tendon/ligament bone anchor, non-bioabsorbable

GRYPHON Flex by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament bone anchor, non-bioabsorbable.

Cleared under the same submission

K232492 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 94b96a63-2e39-406b-b19c-aa04937d9ef5 36 fields · synced Jun 1, 2026