← Back to catalogue

Movement®

FDA UDI

Class II (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
Movement® FDA UDI
Generic Name
Surgical implant template, reusable FDA UDI
Device Name
The Movement Great Toe proximal phalanx implant sizer allows for clear visualization of the implant size. FDA UDI
Model / Reference
PIS89000 FDA UDI
Description
The Movement Great Toe proximal phalanx implant sizer allows for clear visualization of the implant size. FDA UDI

Identifiers

Primary DI / UDI-DI
10381780237150 FDA UDI
510(k) Number
K092047 FDA UDI
FDA Product Code
KWD FDA UDI
GMDN Term
Surgical implant template, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical implant template, reusable

Movement® by Ascension Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant template, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c24eb69a-affc-4803-b2f0-e4e8910730d8 37 fields · synced May 30, 2026