FDA Device Intelligence
Home › Hausmann Enterprises, LLC › TABLE,TREATMENT,H-BRACE

TABLE,TREATMENT,H-BRACE

Hausmann Enterprises, LLC · Model 4020-99 · UDI-DI 00840314811059

INT
4
510(k) clearances
1
Adverse events
5
Recalls
9
Facilities

Description

TABLE,TREATMENT,H-BRACE SKU 4020-99

Recalls

DateFirmReason
2006-01-25SAMMONS PRESTON ROLYANThere have been reports of structural failure on the skirt of select tables. The risk to patients presented by possible structural failure of the skirt of the table is a slow coll
2006-01-25SAMMONS PRESTON ROLYANThere have been reports of structural failure on the skirt of select tables. The risk to patients presented by possible structural failure of the skirt of the table is a slow coll
2006-01-25SAMMONS PRESTON ROLYANThere have been reports of structural failure on the skirt of select tables. The risk to patients presented by possible structural failure of the skirt of the table is a slow coll
2006-01-25SAMMONS PRESTON ROLYANThere have been reports of structural failure on the skirt of select tables. The risk to patients presented by possible structural failure of the skirt of the table is a slow coll
2006-01-25SAMMONS PRESTON ROLYANThere have been reports of structural failure on the skirt of select tables. The risk to patients presented by possible structural failure of the skirt of the table is a slow coll

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.