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PunchTac 5.5mm Anchor PEEK

FDA UDI

Class II (US FDA UDI)

by Dunamis Medical LLC

Identity

Trade Name
PunchTac 5.5mm Anchor PEEK FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Device Name
5.5mm PunchTac™ Threaded Anchor PEEK Preloaded with Two 2mm DFX Tensile Tape (UHMWPE) Sterile | Single Use FDA UDI
Model / Reference
DFX0035A FDA UDI
Description
5.5mm PunchTac™ Threaded Anchor PEEK Preloaded with Two 2mm DFX Tensile Tape (UHMWPE) Sterile | Single Use FDA UDI

Identifiers

Catalog Number
DFX0035A FDA UDI
Primary DI / UDI-DI
00854629006253 FDA UDI
510(k) Number
K160996 FDA UDI
FDA Product Code
MBI FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

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 Safe FDA UDI

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

PunchTac 5.5mm Anchor PEEK by Dunamis Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw, non-bioabsorbable, sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dunamis Medical LLC

Sources (1)

  • FDA UDI 8d9d2c79-2dac-41a0-a6b5-9b898282c90d 36 fields · synced May 30, 2026