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Morphix

FDA UDI

Class II (US FDA UDI)

by Medshape, Inc.

Identity

Trade Name
Morphix FDA UDI
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name
MORPHIX 5.5mm x 11mm Anchor with three sutures FDA UDI
Model / Reference
1000-03-355 FDA UDI
Description
MORPHIX 5.5mm x 11mm Anchor with three sutures FDA UDI

Identifiers

Primary DI / UDI-DI
M9701000033550 FDA UDI
510(k) Number
K091202 FDA UDI
FDA Product Code
HWC FDA UDI
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

Morphix by Medshape, Inc. — 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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medshape, Inc.

Sources (1)

  • FDA UDI 04ce66c5-38c8-4628-8db8-d043ccbd49d3 34 fields · synced May 30, 2026