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DynaClip Delta

FDA UDI

Class II (US FDA UDI)

by Medshape, Inc.

Identity

Trade Name
DynaClip Delta FDA UDI
Generic Name
Orthopaedic bone staple, non-adjustable FDA UDI
Device Name
DELTA DYNACLIP STAPLE, 24X16X14X12 FDA UDI
Model / Reference
3000-10-24161412 FDA UDI
Description
DELTA DYNACLIP STAPLE, 24X16X14X12 FDA UDI

Identifiers

Primary DI / UDI-DI
M970300010241614120 FDA UDI
510(k) Number
K220812 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
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic bone staple, non-adjustable

DynaClip Delta by Medshape, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone staple, non-adjustable.

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 1c508bbf-6f72-4336-843d-1ff38324e83c 34 fields · synced Jun 1, 2026