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Flower Orthopedics

FDA UDI

Class I (US FDA UDI)

by Flower Orthopedics Corporation

Identity

Trade Name
Flower Orthopedics FDA UDI
Generic Name
Bone tack inserter, basic FDA UDI
Device Name
Plate Tack, Medium FDA UDI
Model / Reference
PTK 200 FDA UDI
Description
Plate Tack, Medium FDA UDI

Identifiers

Primary DI / UDI-DI
00840118125185 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone tack inserter, basic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Bone tack inserter, basic

Flower Orthopedics by Flower Orthopedics Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tack inserter, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ca67d31d-db1e-46c8-9a30-f662b88a5869 34 fields · synced Jun 6, 2026