← Back to catalogue

TrellOss™-A

FDA UDI

Class II (US FDA UDI)

by Nexxt Spine Llc

Identity

Trade Name
TrellOss™-A FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
ALIF, Tray ALIF Insertion FDA UDI
Model / Reference
300H2001 FDA UDI
Description
ALIF, Tray ALIF Insertion FDA UDI

Identifiers

Primary DI / UDI-DI
00840067204948 FDA UDI
510(k) Number
K193370 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 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: Device sterilization/disinfection container, reusable

TrellOss™-A by Nexxt Spine Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, 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

Manufacturer
Nexxt Spine Llc

Sources (1)

  • FDA UDI d2fdb6eb-4342-4de2-8922-27ca13075051 35 fields · synced Jun 6, 2026