FDA applicant

Center For Biomaterials and Advanced Technologies

Beltsville, MD1 decision2002–20020 recalls

FDA records 1 decision for Center For Biomaterials and Advanced Technologies (Beltsville, MD) in 2002: 1 510(k) clearance. All are in product code FTL (Mesh, Surgical, Polymeric). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Center For Biomaterials and Advanced Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Center For Biomaterials and Advanced Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Center For Biomaterials and Advanced Technologies by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Center”

FDA records each applicant name separately; these may or may not be the same firm.

Center Laboratories, Inc. 2 Center For Marketing Services 1 The Center For Craniofacial & Dental Sleep Medicine 1 Center For Orthotic and Prosthetic Care,Llc 1 Center For Disease Control and Prevention (Cdc) 1

Center For Biomaterials and Advanced Technologies

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Center”