ACE Acetabular Reamer 39mm 50141039

by Incipio Devices GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number07630055305282 UDI-DI	Date30 Apr 2025Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name: ACE Acetabular Reamer 39mm
Generic Name: Acetabular orthopaedic reamer
Model / Ref / Catalog: 50141039, 00-501-410-39

Primary DI / UDI-DI: 07630055305282
FDA Product Code: HTO
GMDN Term: Acetabular orthopaedic reamer

Device Class: Class I
Regulation Number: 888.4540
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

Size: Outer Diameter — 39 Millimeter

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Properties

Prescription Use
Premarket Exempt
Lot / Batch Number
Manufacturing Date

Other properties (10)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No
Expiration Date: No