Aztec 10-15621

by Aztecmed/Ent LLC

Aztec 10-15621 is a Class I device made by Aztecmed/Ent LLC, listed in FDA GUDID since 6 Oct 2020 (UDI-DI B87110156210), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberB87110156210 UDI-DI	Date6 Oct 2020Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Aztec
Generic name: Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Model / Ref / Catalog: 10-15621

Primary DI / UDI-DI: B87110156210
FDA product code: KAE
GMDN term: Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Device class: Class I
Regulation number: 874.4420
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Premarket exempt

Other properties (13, all answered No)