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AutoPose Access

FDA UDI

Class II (US FDA UDI)

by Bimini Technologies LLC

Identity

Trade Name
AutoPose Access FDA UDI
Generic Name
Resective skin contouring/liposuction system depth guide FDA UDI
Device Name
A pre-assembled, sterile, single use system intended to assist the harvesting of autologous fat grafts from a patient for aesthetic body contouring. It creates a guided incision for cannula introduction at a controlled depth (10 mm) under the skin for the purpose of small volume adipose tissue harvest. FDA UDI
Model / Reference
ABS-101024-1 FDA UDI
Description
A pre-assembled, sterile, single use system intended to assist the harvesting of autologous fat grafts from a patient for aesthetic body contouring. It creates a guided incision for cannula introduction at a controlled depth (10 mm) under the skin for the purpose of small volume adipose tissue harvest. FDA UDI

Identifiers

Primary DI / UDI-DI
00850034511320 FDA UDI
FDA Product Code
MUU FDA UDI
GMDN Term
Resective skin contouring/liposuction system depth guide FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5040 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

Category: Resective skin contouring/liposuction system depth guide

AutoPose Access by Bimini Technologies LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 50c6c49a-43dd-45c8-90e3-3bead3c864dc 33 fields · synced Jun 1, 2026