← Back to catalogue

OsteoMed

FDA UDI

Class II (US FDA UDI)

by Osteomed Corp.

Identity

Trade Name
OsteoMed FDA UDI
Generic Name
Orthopaedic bone staple, non-adjustable FDA UDI
Device Name
InstaFix Sizers Kit FDA UDI
Model / Reference
400-7777-SP FDA UDI
Description
InstaFix Sizers Kit FDA UDI

Identifiers

Catalog Number
400-7777-SP FDA UDI
Primary DI / UDI-DI
00842528104279 FDA UDI
FDA Product Code
JDR FDA UDI
GMDN Term
Orthopaedic bone staple, non-adjustable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

Dimensions & Sizes

Size
Length — 7 Millimeter FDA UDI

Category: Orthopaedic bone staple, non-adjustable

A comprehensive medical device directory listing for OsteoMed Orthopaedic bone staple, non-adjustable (InstaFix Sizers Kit)

Similar devices

Also classified as Orthopaedic bone staple, non-adjustable.

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

Manufacturer
Osteomed Corp.

Sources (1)

  • FDA UDI e48e652a-4adc-4fec-86f7-b67392d56f4c 36 fields · synced Jul 9, 2026