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Panta

FDA UDI

Class II (US FDA UDI)

by Newdeal Sas

Identity

Trade Name
PANTA FDA UDI
Generic Name
Bone nail end-cap FDA UDI
Device Name
The end cap is made from Titanium alloy and may be inserted into the distal nail threads to prevent tissue ingrowth and facilitate future nail removal. FDA UDI
Model / Reference
500001ND FDA UDI
Description
The end cap is made from Titanium alloy and may be inserted into the distal nail threads to prevent tissue ingrowth and facilitate future nail removal. FDA UDI

Identifiers

Catalog Number
500001ND FDA UDI
Primary DI / UDI-DI
10381780044482 FDA UDI
510(k) Number
K050882 FDA UDI
K091788 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Bone nail end-cap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 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

Yes

FDA UDI

Category: Bone nail end-cap

Panta by Newdeal Sas — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone nail end-cap.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Newdeal Sas

Sources (1)

  • FDA UDI 9138e007-3318-4a21-ae60-120b3c354875 39 fields · synced Jun 7, 2026