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Integrity Orthopaedics

FDA UDI

Class II (US FDA UDI)

by Integrity Orthopaedics, Inc.

Identity

Trade Name
Integrity Orthopaedics FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, single-use FDA UDI
Device Name
Tendon Seam™ Instrument Kit - 4 Anchor FDA UDI
Model / Reference
901005 FDA UDI
Description
Tendon Seam™ Instrument Kit - 4 Anchor FDA UDI

Identifiers

Catalog Number
901005 FDA UDI
Primary DI / UDI-DI
00860013905972 FDA UDI
FDA Product Code
MBI FDA UDI
LXH FDA UDI
GMDN Term
Orthopaedic inorganic implant inserter/extractor, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

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

Category: Tendon/ligament bone anchor, non-bioabsorbableOrthopaedic inorganic implant inserter/extractor, single-use

Integrity Orthopaedics by Integrity Orthopaedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic inorganic implant inserter/extractor, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI da702c09-8eae-45f1-9b99-3e46a3500710 34 fields · synced Jun 1, 2026